메뉴 건너뛰기




Volumn 135, Issue 5, 2015, Pages 1132-1141

Advances in basic and clinical immunology in 2014

Author keywords

common variable immunodeficiency; dedicator of cytokinesis 8; HIV1; Immunology; intravenous immunoglobulin; newborn screening; primary immunodeficiency; recombination activating gene 1; severe combined immunodeficiency

Indexed keywords

IMMUNOGLOBULIN; PEGINTERFERON ALPHA2B;

EID: 84937512383     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2015.02.037     Document Type: Review
Times cited : (17)

References (102)
  • 1
    • 84905487884 scopus 로고    scopus 로고
    • The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency
    • S.E. Turvey, A. Durandy, A. Fischer, S.Y. Fung, R.S. Geha, A. Gewies, and et al. The CARD11-BCL10-MALT1 (CBM) signalosome complex: stepping into the limelight of human primary immunodeficiency J Allergy Clin Immunol 134 2014 276 284
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 276-284
    • Turvey, S.E.1    Durandy, A.2    Fischer, A.3    Fung, S.Y.4    Geha, R.S.5    Gewies, A.6
  • 3
  • 4
    • 84914166384 scopus 로고    scopus 로고
    • Intact IL-12 signaling is necessary for the generation of human natural killer cells with enhanced effector function after restimulation
    • V.R. Simhadri, M.L. Mariano, O. Zemarruzabeitia, C.M. Seroogy, S.M. Holland, H.S. Kuehn, and et al. Intact IL-12 signaling is necessary for the generation of human natural killer cells with enhanced effector function after restimulation J Allergy Clin Immunol 134 2014 1190 1193.e1
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1190-1193e1
    • Simhadri, V.R.1    Mariano, M.L.2    Zemarruzabeitia, O.3    Seroogy, C.M.4    Holland, S.M.5    Kuehn, H.S.6
  • 5
    • 84903733656 scopus 로고    scopus 로고
    • MicroRNA-150 regulates the cytotoxicity of natural killers by targeting perforin-1
    • N. Kim, M. Kim, S. Yun, J. Doh, P.D. Greenberg, T.D. Kim, and et al. MicroRNA-150 regulates the cytotoxicity of natural killers by targeting perforin-1 J Allergy Clin Immunol 134 2014 195 203
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 195-203
    • Kim, N.1    Kim, M.2    Yun, S.3    Doh, J.4    Greenberg, P.D.5    Kim, T.D.6
  • 6
    • 84905562170 scopus 로고    scopus 로고
    • Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia and multiple sclerosis
    • H. Sic, H. Kraus, J. Madl, K.A. Flittner, A.L. von Muschow, K. Pieper, and et al. Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia and multiple sclerosis J Allergy Clin Immunol 134 2014 420 428
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 420-428
    • Sic, H.1    Kraus, H.2    Madl, J.3    Flittner, K.A.4    Von Muschow, A.L.5    Pieper, K.6
  • 9
    • 84903730984 scopus 로고    scopus 로고
    • Human CD19 and CD40L deficiencies impair antibody selection and differentially affect somatic hypermutation
    • M.C. Van Zelm, S.J. Bartol, G.J. Driessen, F. Mascart, I. Reisli, J.L. Franco, and et al. Human CD19 and CD40L deficiencies impair antibody selection and differentially affect somatic hypermutation J Allergy Clin Immunol 134 2014 135 144
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 135-144
    • Van Zelm, M.C.1    Bartol, S.J.2    Driessen, G.J.3    Mascart, F.4    Reisli, I.5    Franco, J.L.6
  • 10
    • 84897421218 scopus 로고    scopus 로고
    • Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development
    • X. Yu, J.R. Almeida, S. Darko, M. van der Burg, S.S. Ravin, H. Malech, and et al. Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development J Allergy Clin Immunol 133 2014 1109 1115
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1109-1115
    • Yu, X.1    Almeida, J.R.2    Darko, S.3    Van Der Burg, M.4    Ravin, S.S.5    Malech, H.6
  • 13
    • 84897386968 scopus 로고    scopus 로고
    • Signaling lymphocyte activation molecule associated protein (SAP) pathway regulates human B cell tolerance
    • L. Menard, T. Caekert, N. Chamberlain, S.G. Tangye, S. Riminton, J.A. Church, and et al. Signaling lymphocyte activation molecule associated protein (SAP) pathway regulates human B cell tolerance J Allergy Clin Immunol 133 2014 1149 1161
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1149-1161
    • Menard, L.1    Caekert, T.2    Chamberlain, N.3    Tangye, S.G.4    Riminton, S.5    Church, J.A.6
  • 14
    • 84908440532 scopus 로고    scopus 로고
    • Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells
    • E. Janssen, H. Morbach, S. Ullas, J.M. Bannock, C. Massad, L. Menard, and et al. Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells J Allergy Clin Immunol 134 2014 1365 1374
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1365-1374
    • Janssen, E.1    Morbach, H.2    Ullas, S.3    Bannock, J.M.4    Massad, C.5    Menard, L.6
  • 15
    • 84905591094 scopus 로고    scopus 로고
    • Dysregulated extracellular signal-regulated kinase signaling associated with impaired B-cell receptor endocytosis in patients with common variable immunodeficiency
    • M. Visentine, R. Marrapodi, V. Conti, M. Mitrevski, A. Camponeschi, C. Lazzeri, and et al. Dysregulated extracellular signal-regulated kinase signaling associated with impaired B-cell receptor endocytosis in patients with common variable immunodeficiency J Allergy Clin Immunol 134 2014 401 410
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 401-410
    • Visentine, M.1    Marrapodi, R.2    Conti, V.3    Mitrevski, M.4    Camponeschi, A.5    Lazzeri, C.6
  • 16
    • 84897469677 scopus 로고    scopus 로고
    • A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency
    • K. Pieper, M. Rizzi, M. Spelatas, C. Smulski, H. Sic, H. Kraus, and et al. A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency J Allergy Clin Immunol 133 2014 1222 1225
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1222-1225
    • Pieper, K.1    Rizzi, M.2    Spelatas, M.3    Smulski, C.4    Sic, H.5    Kraus, H.6
  • 18
    • 84901804635 scopus 로고    scopus 로고
    • CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation
    • C.M. Buckner, S. Moir, L. Kardava, J. Ho, B.H. Santich, L.J. Kim, and et al. CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation J Allergy Clin Immunol 133 2014 1676 1685
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1676-1685
    • Buckner, C.M.1    Moir, S.2    Kardava, L.3    Ho, J.4    Santich, B.H.5    Kim, L.J.6
  • 19
    • 84896730732 scopus 로고    scopus 로고
    • TH17 differentiation capacity develops within the first 3 months of life
    • K.K. Dijkstra, S.B. Hoeks, B.J. Prokken, and S. deRoeck TH17 differentiation capacity develops within the first 3 months of life J Allergy Clin Immunol 133 2014 891 894.e5
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 891-894e5
    • Dijkstra, K.K.1    Hoeks, S.B.2    Prokken, B.J.3    DeRoeck, S.4
  • 23
    • 84899618667 scopus 로고    scopus 로고
    • Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
    • Y. Zhang, X. Yu, M. Ichikawa, J.J. Lyons, S. Datta, I.T. Lamborn, H. Jing, and et al. Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment J Allergy Clin Immunol 133 2014 1400 1409
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1400-1409
    • Zhang, Y.1    Yu, X.2    Ichikawa, M.3    Lyons, J.J.4    Datta, S.5    Lamborn, I.T.6    Jing, H.7
  • 24
    • 84904036824 scopus 로고    scopus 로고
    • PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia
    • A. Stray-Pedersen, P.H. Backe, H.S. Sorte, L. Mørkrid, N.Y. Chokshi, H.C. Erichsen, and et al. PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia Am J Hum Genet 95 2014 96 107
    • (2014) Am J Hum Genet , vol.95 , pp. 96-107
    • Stray-Pedersen, A.1    Backe, P.H.2    Sorte, H.S.3    Mørkrid, L.4    Chokshi, N.Y.5    Erichsen, H.C.6
  • 25
    • 84899629014 scopus 로고    scopus 로고
    • Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels
    • A. Sassi, S. Lazaroski, G. Wu, S.M. Haslam, M. Fliegauf, F. Mellouli, and et al. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels J Allergy Clin Immunol 133 2014 1410 1419
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1410-1419
    • Sassi, A.1    Lazaroski, S.2    Wu, G.3    Haslam, S.M.4    Fliegauf, M.5    Mellouli, F.6
  • 26
    • 84901778963 scopus 로고    scopus 로고
    • Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency
    • E. Salzer, A. Kansu, H. Sic, P. Majek, A. Ikinciogullari, F.E. Dogu, and et al. Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency J Allergy Clin Immunol 133 2014 1651 1659.e12
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1651-1659e12
    • Salzer, E.1    Kansu, A.2    Sic, H.3    Majek, P.4    Ikinciogullari, A.5    Dogu, F.E.6
  • 27
    • 84938070889 scopus 로고    scopus 로고
    • Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations
    • D. Schubert, C. Bode, R. Kenefeck, T.Z. Hou, J.B. Wing, A. Kennedy, and et al. Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations Nat Med 20 2014 1410 1416
    • (2014) Nat Med , vol.20 , pp. 1410-1416
    • Schubert, D.1    Bode, C.2    Kenefeck, R.3    Hou, T.Z.4    Wing, J.B.5    Kennedy, A.6
  • 28
    • 84907909000 scopus 로고    scopus 로고
    • Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4
    • H.S. Kuehn, W. Ouyang, B. Lo, E.K. Deenick, J.E. Niemela, D.T. Avery, and et al. Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4 Science 345 2014 1623 1627
    • (2014) Science , vol.345 , pp. 1623-1627
    • Kuehn, H.S.1    Ouyang, W.2    Lo, B.3    Deenick, E.K.4    Niemela, J.E.5    Avery, D.T.6
  • 30
    • 84921847830 scopus 로고    scopus 로고
    • Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K
    • C.L. Lucas, Y. Zhang, A. Venida, Y. Wang, J. Hughes, J. McElwee, and et al. Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K J Exp Med 211 2014 2537 2547
    • (2014) J Exp Med , vol.211 , pp. 2537-2547
    • Lucas, C.L.1    Zhang, Y.2    Venida, A.3    Wang, Y.4    Hughes, J.5    McElwee, J.6
  • 31
    • 84923384476 scopus 로고    scopus 로고
    • Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity
    • K.L. Willmann, S. Klaver, F. Doʇu, E. Santos-Valente, W. Garncarz, I. Bilic, and et al. Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity Nat Commun 5 2014 5360
    • (2014) Nat Commun , vol.5 , pp. 5360
    • Willmann, K.L.1    Klaver, S.2    Doʇu, F.3    Santos-Valente, E.4    Garncarz, W.5    Bilic, I.6
  • 33
    • 84902342846 scopus 로고    scopus 로고
    • CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
    • E. Martin, N. Palmic, S. Sanquer, C. Lenoir, F. Hauck, C. Mongellaz, and et al. CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation Nature 510 2014 288 292
    • (2014) Nature , vol.510 , pp. 288-292
    • Martin, E.1    Palmic, N.2    Sanquer, S.3    Lenoir, C.4    Hauck, F.5    Mongellaz, C.6
  • 34
    • 84922393563 scopus 로고    scopus 로고
    • JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia
    • K. Boztug, P.M. Järvinen, E. Salzer, T. Racek, S. Mönch, W. Garncarz, and et al. JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia Nat Genet 46 2014 1021 1027
    • (2014) Nat Genet , vol.46 , pp. 1021-1027
    • Boztug, K.1    Järvinen, P.M.2    Salzer, E.3    Racek, T.4    Mönch, S.5    Garncarz, W.6
  • 36
    • 84911922142 scopus 로고    scopus 로고
    • An inherited mutation in NLRC4 causes autoinflammation in human and mice
    • A. Kitamura, Y. Sasaki, T. Abe, H. Kano, and K. Yasutomo An inherited mutation in NLRC4 causes autoinflammation in human and mice J Exp Med 211 2014 2385 2396
    • (2014) J Exp Med , vol.211 , pp. 2385-2396
    • Kitamura, A.1    Sasaki, Y.2    Abe, T.3    Kano, H.4    Yasutomo, K.5
  • 38
    • 84927126118 scopus 로고    scopus 로고
    • An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome
    • S.W. Canna, A.A. de Jesus, S. Gouni, S.R. Brooks, B. Marrero, Y. Liu, and et al. An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome Nat Genet 46 2014 1140 1146
    • (2014) Nat Genet , vol.46 , pp. 1140-1146
    • Canna, S.W.1    De Jesus, A.A.2    Gouni, S.3    Brooks, S.R.4    Marrero, B.5    Liu, Y.6
  • 42
    • 84908584244 scopus 로고    scopus 로고
    • Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)
    • P.K. Chakraborty, K. Schmitz-Abe, E.K. Kennedy, H. Mamady, T. Naas, D. Durie, and et al. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) Blood 124 2014 2867 2871
    • (2014) Blood , vol.124 , pp. 2867-2871
    • Chakraborty, P.K.1    Schmitz-Abe, K.2    Kennedy, E.K.3    Mamady, H.4    Naas, T.5    Durie, D.6
  • 43
    • 84919599348 scopus 로고    scopus 로고
    • Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome due to tetratricopeptide repeat domain 7A deficiency
    • R. Lemoine, J. Pachlopnik-Schmid, H.F. Farin, A. Bigorgne, M. Debre, M. Sepulveda, and et al. Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome due to tetratricopeptide repeat domain 7A deficiency J Allergy Clin Immunol 134 2014 1354 1364
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1354-1364
    • Lemoine, R.1    Pachlopnik-Schmid, J.2    Farin, H.F.3    Bigorgne, A.4    Debre, M.5    Sepulveda, M.6
  • 44
    • 84896729331 scopus 로고    scopus 로고
    • Fatal combined immunodeficiency associated with heterozygous mutation in STAT1
    • N. Sharfe, A. Nahum, A. Newell, H. Dadi, B. Ngan, S.L. Pereira, and et al. Fatal combined immunodeficiency associated with heterozygous mutation in STAT1 J Allergy Clin Immunol 133 2014 807 817
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 807-817
    • Sharfe, N.1    Nahum, A.2    Newell, A.3    Dadi, H.4    Ngan, B.5    Pereira, S.L.6
  • 45
    • 84909643087 scopus 로고    scopus 로고
    • Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100
    • C.E. Lee, D.A. Fulcher, B. Whittle, R. Chand, N. Fewings, M. Field, and et al. Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100 Blood 124 2014 2964 2972
    • (2014) Blood , vol.124 , pp. 2964-2972
    • Lee, C.E.1    Fulcher, D.A.2    Whittle, B.3    Chand, R.4    Fewings, N.5    Field, M.6
  • 46
    • 84901500584 scopus 로고    scopus 로고
    • Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKb
    • S.O. Burns, V. Plagnol, B.M. Gutierrez, D. Al-Zahrani, J. Curtis, M. Gaspar, and et al. Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKb J Allergy Clin Immunol 134 2014 215 218
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 215-218
    • Burns, S.O.1    Plagnol, V.2    Gutierrez, B.M.3    Al-Zahrani, D.4    Curtis, J.5    Gaspar, M.6
  • 47
    • 84914159176 scopus 로고    scopus 로고
    • Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers
    • C. Aguilar, C. Lenoir, N. Lambert, B. Begue, N. Brousse, D. Canioni, and et al. Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers J Allergy Clin Immunol 134 2014 1131 1142
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1131-1142
    • Aguilar, C.1    Lenoir, C.2    Lambert, N.3    Begue, B.4    Brousse, N.5    Canioni, D.6
  • 48
    • 84897412977 scopus 로고    scopus 로고
    • Kindlin 3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III
    • E. van de Vijver, A.T. Tool, O. Sanal, M. Cetin, S. Unal, S. Aytac, and et al. Kindlin 3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III J Allergy Clin Immunol 133 2014 1215 1218
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1215-1218
    • Van De Vijver, E.1    Tool, A.T.2    Sanal, O.3    Cetin, M.4    Unal, S.5    Aytac, S.6
  • 49
    • 84897396302 scopus 로고    scopus 로고
    • Vaccine strain varicella-zoster virus-induced central nervous system vasculopathy as the presenting feature of DOCK8 deficiency
    • A. Sabry, P.J. Hauk, H. Jing, H.C. Su, N.V. Stence, D.M. Mirsky, and et al. Vaccine strain varicella-zoster virus-induced central nervous system vasculopathy as the presenting feature of DOCK8 deficiency J Allergy Clin Immunol 133 2014 1225 1227
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1225-1227
    • Sabry, A.1    Hauk, P.J.2    Jing, H.3    Su, H.C.4    Stence, N.V.5    Mirsky, D.M.6
  • 52
    • 84904872011 scopus 로고    scopus 로고
    • Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia
    • N.K. Serwas, D. Cagdas, S.A. Ban, K. Bienemann, E. Salzer, I. Tezcan, and et al. Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia Blood 124 2014 655 657
    • (2014) Blood , vol.124 , pp. 655-657
    • Serwas, N.K.1    Cagdas, D.2    Ban, S.A.3    Bienemann, K.4    Salzer, E.5    Tezcan, I.6
  • 53
    • 84891030577 scopus 로고    scopus 로고
    • Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency
    • C.L. Lucas, H.S. Kuehn, F. Zhao, J.E. Niemela, E.K. Deenick, U. Palendira, and et al. Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency Nat Immunol 15 2014 88 97
    • (2014) Nat Immunol , vol.15 , pp. 88-97
    • Lucas, C.L.1    Kuehn, H.S.2    Zhao, F.3    Niemela, J.E.4    Deenick, E.K.5    Palendira, U.6
  • 54
    • 84908147862 scopus 로고    scopus 로고
    • Lessons in gene hunting: A RAG1 mutation presenting with agammaglobulinemia and absence of B cells
    • M. Hadayat, M.J. Masaad, N.Y. Lee, M.E. Conley, J.S. Orange, T.K. Ohsumi, and et al. Lessons in gene hunting: a RAG1 mutation presenting with agammaglobulinemia and absence of B cells J Allergy Clin Immunol 134 2014 983 985
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 983-985
    • Hadayat, M.1    Masaad, M.J.2    Lee, N.Y.3    Conley, M.E.4    Orange, J.S.5    Ohsumi, T.K.6
  • 55
    • 84896710741 scopus 로고    scopus 로고
    • Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations
    • K. Chen, W. Wu, D. Mathew, Y. Zhang, S.K. Browne, L.B. Rosen, and et al. Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations J Allergy Clin Immunol 134 2014 880 882
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 880-882
    • Chen, K.1    Wu, W.2    Mathew, D.3    Zhang, Y.4    Browne, S.K.5    Rosen, L.B.6
  • 56
    • 84919843125 scopus 로고    scopus 로고
    • A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency
    • H. Abolhassani, N. Wang, A. Aghamohammadi, N. Rezaei, Y.N. Lee, F. Frugoni, and et al. A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency J Allergy Clin Immunol 134 2014 1375 1380
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1375-1380
    • Abolhassani, H.1    Wang, N.2    Aghamohammadi, A.3    Rezaei, N.4    Lee, Y.N.5    Frugoni, F.6
  • 57
    • 84897448055 scopus 로고    scopus 로고
    • Lesson from hypomorphic recombinant activating gene (RAG) mutations: Why asymptomatic siblings should be tested
    • C. Schuetz, U. Pannicke, E.M. Jacobsen, S. Burggraf, M.H. Albert, M. Honig, and et al. Lesson from hypomorphic recombinant activating gene (RAG) mutations: why asymptomatic siblings should be tested J Allergy Clin Immunol 133 2014 1211 1215
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1211-1215
    • Schuetz, C.1    Pannicke, U.2    Jacobsen, E.M.3    Burggraf, S.4    Albert, M.H.5    Honig, M.6
  • 58
    • 84897389616 scopus 로고    scopus 로고
    • A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency
    • Y.N. Lee, F. Frugoni, K. Dobbs, J.E. Walter, S. Giliani, A.R. Gennery, and et al. A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency J Allergy Clin Immunol 133 2014 1099 1108
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1099-1108
    • Lee, Y.N.1    Frugoni, F.2    Dobbs, K.3    Walter, J.E.4    Giliani, S.5    Gennery, A.R.6
  • 59
    • 84897444766 scopus 로고    scopus 로고
    • Similar recombination-activating gene (RAG) mutation result in similar immunological effects but in different clinical phenotypes
    • H. IJspeert, G.J. Driessen, M.J. Moorhouse, N.G. Hartwig, B. Wolska-Kunierz, K. Kalwak, and et al. Similar recombination-activating gene (RAG) mutation result in similar immunological effects but in different clinical phenotypes J Allergy Clin Immunol 133 2014 1124 1133
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1124-1133
    • Ijspeert, H.1    Driessen, G.J.2    Moorhouse, M.J.3    Hartwig, N.G.4    Wolska-Kunierz, B.5    Kalwak, K.6
  • 60
    • 84905502530 scopus 로고    scopus 로고
    • Gene hunting in the genomic era: Approaches to diagnostic dilemmas in patients with primary immunodeficiencies
    • C. Platt, R.S. Geha, and J. Chou Gene hunting in the genomic era: approaches to diagnostic dilemmas in patients with primary immunodeficiencies J Allergy Clin Immunol 134 2014 262 268
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 262-268
    • Platt, C.1    Geha, R.S.2    Chou, J.3
  • 64
    • 85027940542 scopus 로고    scopus 로고
    • Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease
    • A. Magnani, P. Brosselin, J. Beaute, N. de Vergnes, R. Mouy, M. Debre, and et al. Inflammatory manifestations in a single-center cohort of patients with chronic granulomatous disease J Allergy Clin Immunol 134 2014 655 662.e8
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 655-662e8
    • Magnani, A.1    Brosselin, P.2    Beaute, J.3    De Vergnes, N.4    Mouy, R.5    Debre, M.6
  • 66
    • 84899622887 scopus 로고    scopus 로고
    • Common variable immunodeficiency is associated with a functional deficiency of invariant natural killer cells
    • Y. Gao, S. Workmann, S. Gadola, T. Elliott, B. Grimbacher, and A.P. Williams Common variable immunodeficiency is associated with a functional deficiency of invariant natural killer cells J Allergy Clin Immunol 134 2014 1420 1428
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1420-1428
    • Gao, Y.1    Workmann, S.2    Gadola, S.3    Elliott, T.4    Grimbacher, B.5    Williams, A.P.6
  • 67
    • 84895064377 scopus 로고    scopus 로고
    • Tertiary lymphoid neogenesis is a component of pulmonary lymphoid hyperplasia in patients with common variable immunodeficiency
    • P.J. Maglione, H.M. Ko, M.B. Beasley, J.A. Strauchen, and C. Cunningham-Rundles Tertiary lymphoid neogenesis is a component of pulmonary lymphoid hyperplasia in patients with common variable immunodeficiency J Allergy Clin Immunol 134 2014 535 542
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 535-542
    • Maglione, P.J.1    Ko, H.M.2    Beasley, M.B.3    Strauchen, J.A.4    Cunningham-Rundles, C.5
  • 68
    • 84903746318 scopus 로고    scopus 로고
    • Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome
    • S. Kracker, J. Curtis, M.A. Ibrahim, A. Sediva, J. Salisbury, V. Campr, and et al. Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome J Allergy Clin Immunol 134 2014 233 236
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 233-236
    • Kracker, S.1    Curtis, J.2    Ibrahim, M.A.3    Sediva, A.4    Salisbury, J.5    Campr, V.6
  • 69
    • 84895056711 scopus 로고    scopus 로고
    • A novel mutation in IFN-g receptor 1 presenting as multisystem Mycobacteium intracellulare infection
    • D.M. Rose, J. Atkins, S.M. Holland, and A.J. Infante A novel mutation in IFN-g receptor 1 presenting as multisystem Mycobacteium intracellulare infection J Allergy Clin Immunol 134 2014 591 592
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 591-592
    • Rose, D.M.1    Atkins, J.2    Holland, S.M.3    Infante, A.J.4
  • 70
    • 84901777686 scopus 로고    scopus 로고
    • Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype
    • H. Jing, Q. Zhang, Y. Zhang, B.J. Hill, C.G. Dove, E.W. Gelfand, and et al. Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype J Allergy Clin Immunol 133 2014 1667 1675
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1667-1675
    • Jing, H.1    Zhang, Q.2    Zhang, Y.3    Hill, B.J.4    Dove, C.G.5    Gelfand, E.W.6
  • 71
    • 84903692809 scopus 로고    scopus 로고
    • A case of partial dedicators of cytokinesis 8 deficiency with altered effector phenotype and impaired CD8+ and natural killer cytotoxicity
    • R. Ruiz-Garcia, S. Lermo-Rojo, L. Martinez-Lostao, E. Mancebo, S. Mora-Diaz, S. Paz-Artal, and et al. A case of partial dedicators of cytokinesis 8 deficiency with altered effector phenotype and impaired CD8+ and natural killer cytotoxicity J Allergy Clin Immunol 134 2014 218 221
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 218-221
    • Ruiz-Garcia, R.1    Lermo-Rojo, S.2    Martinez-Lostao, L.3    Mancebo, E.4    Mora-Diaz, S.5    Paz-Artal, S.6
  • 72
    • 84914151539 scopus 로고    scopus 로고
    • Gain of function mutations in signal transducer and activator of transcription 1 (STAT1): Chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding
    • G. Frans, L. Moens, H. Schaballie, L. Van Eyck, H. Borgers, M. Wayts, and et al. Gain of function mutations in signal transducer and activator of transcription 1 (STAT1): chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding J Allergy Clin Immunol 134 2014 1209 1212
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1209-1212
    • Frans, G.1    Moens, L.2    Schaballie, H.3    Van Eyck, L.4    Borgers, H.5    Wayts, M.6
  • 73
    • 84896709292 scopus 로고    scopus 로고
    • Penicillium marneffei infection and impaired IFNγ immunity in humans with autosomal-dominant gain of phosphorylation STAT1 mutations
    • P.P.W. Lee, H. Mao, W. Yang, K.W. Can, M.H. Ko, J.F. Chan, and et al. Penicillium marneffei infection and impaired IFNγ immunity in humans with autosomal-dominant gain of phosphorylation STAT1 mutations J Allergy Clin Immunol 134 2014 894 896.e5
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 894-896e5
    • Lee, P.P.W.1    Mao, H.2    Yang, W.3    Can, K.W.4    Ko, M.H.5    Chan, J.F.6
  • 74
    • 84903734036 scopus 로고    scopus 로고
    • Gain of function signal transducer and activator of transcription 1 (STAT1) mutation-related primary immunodeficiency is associated with disseminated mucormycosis
    • N. Kumar, M.E. Hanks, P. Chandrasekan, B.C. Davis, A.P. Hsu, N.J. Van Wagoner, and et al. Gain of function signal transducer and activator of transcription 1 (STAT1) mutation-related primary immunodeficiency is associated with disseminated mucormycosis J Allergy Clin Immunol 134 2014 236 239
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 236-239
    • Kumar, N.1    Hanks, M.E.2    Chandrasekan, P.3    Davis, B.C.4    Hsu, A.P.5    Van Wagoner, N.J.6
  • 75
    • 84896722382 scopus 로고    scopus 로고
    • CARD9 mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiency
    • X. Wang, W. Wang, Z. Lin, X. Wang, T. Li, J. Yu, and et al. CARD9 mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiency J Allergy Clin Immunol 133 2014 905 908
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 905-908
    • Wang, X.1    Wang, W.2    Lin, Z.3    Wang, X.4    Li, T.5    Yu, J.6
  • 76
    • 84906543118 scopus 로고    scopus 로고
    • Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States
    • A. Kwan, R.S. Abraham, R. Currier, A. Brower, K. Andruszewski, J.K. Abbott, and et al. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States JAMA 312 2014 729 738
    • (2014) JAMA , vol.312 , pp. 729-738
    • Kwan, A.1    Abraham, R.S.2    Currier, R.3    Brower, A.4    Andruszewski, K.5    Abbott, J.K.6
  • 77
    • 84903705060 scopus 로고    scopus 로고
    • Diagnosis of immunodeficiency phosphorylase defect by using tandem mass spectrometry in dried blood spots
    • G. La Marca, C. Canessa, E. Giocaliere, F. Romano, S. Malvagia, S. Funghini, and et al. Diagnosis of immunodeficiency phosphorylase defect by using tandem mass spectrometry in dried blood spots J Allergy Clin Immunol 134 2014 155 159
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 155-159
    • La Marca, G.1    Canessa, C.2    Giocaliere, E.3    Romano, F.4    Malvagia, S.5    Funghini, S.6
  • 78
    • 84903731039 scopus 로고    scopus 로고
    • Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B cell immunodeficiencies
    • S. Borte, M. Meeths, I. Liebschert, K. Krist, M. Norsdenkjold, L. Hammarstrom, and et al. Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B cell immunodeficiencies J Allergy Clin Immunol 134 2014 226 228
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 226-228
    • Borte, S.1    Meeths, M.2    Liebschert, I.3    Krist, K.4    Norsdenkjold, M.5    Hammarstrom, L.6
  • 81
    • 84897417058 scopus 로고    scopus 로고
    • Establishing diagnostic criteria for severe combined immunodeficiency (SCID), leaky SCID and Omenn syndrome: The Primary Immune Deficiency Treatment Consortium experience
    • W.T. Shearer, E. Dunn, L.D. Notarangelo, C.C. Dvorak, J.M. Puck, B.R. Logan, and et al. Establishing diagnostic criteria for severe combined immunodeficiency (SCID), leaky SCID and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience J Clin Allergy Immunol 133 2014 1092 1098
    • (2014) J Clin Allergy Immunol , vol.133 , pp. 1092-1098
    • Shearer, W.T.1    Dunn, E.2    Notarangelo, L.D.3    Dvorak, C.C.4    Puck, J.M.5    Logan, B.R.6
  • 83
    • 84908123060 scopus 로고    scopus 로고
    • Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency
    • C.C. Dvorak, A. Hassan, M.A. Slatter, M. Honig, A.C. Lankester, R.H. Buckley, and et al. Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency J Allergy Clin Immunol 134 2014 935 943
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 935-943
    • Dvorak, C.C.1    Hassan, A.2    Slatter, M.A.3    Honig, M.4    Lankester, A.C.5    Buckley, R.H.6
  • 85
    • 84901804522 scopus 로고    scopus 로고
    • Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency
    • A. Hassan, P. Lee, P. Maggina, J.H. Xu, D. Moreira, M. Slatter, and et al. Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency J Allergy Clin Immunol 133 2014 1660 1666
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1660-1666
    • Hassan, A.1    Lee, P.2    Maggina, P.3    Xu, J.H.4    Moreira, D.5    Slatter, M.6
  • 86
    • 84919640076 scopus 로고    scopus 로고
    • Severe cutaneous human papilloma virus infection associated with natural killer deficiency following stem cell transplantation for severe combined immunodeficiency
    • Q.U. Kamili, F.O. Seeborg, K. Saxena, S.K. Nicholas, P.P. Banerjee, L.S. Angelo, and et al. Severe cutaneous human papilloma virus infection associated with natural killer deficiency following stem cell transplantation for severe combined immunodeficiency J Allergy Clin Immunol 134 2014 1451 1453.e1
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1451-1453e1
    • Kamili, Q.U.1    Seeborg, F.O.2    Saxena, K.3    Nicholas, S.K.4    Banerjee, P.P.5    Angelo, L.S.6
  • 87
    • 84892636089 scopus 로고    scopus 로고
    • SCID patients with ARTEMIS vs RAG deficiencies following HCT: Increased risk of late toxicity in ARTEMIS-deficient SCID
    • C. Schuetz, B. Neven, C.C. Dvorak, S. Leroy, M.J. Ege, U. Pannicke, and et al. SCID patients with ARTEMIS vs RAG deficiencies following HCT: increased risk of late toxicity in ARTEMIS-deficient SCID Blood 123 2014 281 289
    • (2014) Blood , vol.123 , pp. 281-289
    • Schuetz, C.1    Neven, B.2    Dvorak, C.C.3    Leroy, S.4    Ege, M.J.5    Pannicke, U.6
  • 88
    • 84914102333 scopus 로고    scopus 로고
    • Haploidential T-cell alpha beta receptor and CD19-depleted stem cell transplant for Wiskott Aldrich syndrome
    • G. Kharya, Z. Nademi, T.R. Leahy, J. Dunn, D. Barge, and A. Shulz Haploidential T-cell alpha beta receptor and CD19-depleted stem cell transplant for Wiskott Aldrich syndrome J Allergy Clin Immunol 134 2014 1199 1201
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1199-1201
    • Kharya, G.1    Nademi, Z.2    Leahy, T.R.3    Dunn, J.4    Barge, D.5    Shulz, A.6
  • 89
    • 84914160574 scopus 로고    scopus 로고
    • Circulating endothelial cells as markers of endothelial dysfunction during hematopoietic stem cell transplantation for pediatric primary immunodeficiency
    • F. Touzot, D. Moshous, G. Cros, P. Frange, M. Chornton, M.L. Friedmind, and et al. Circulating endothelial cells as markers of endothelial dysfunction during hematopoietic stem cell transplantation for pediatric primary immunodeficiency J Allergy Clin Immunol 134 2014 1203 1206
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1203-1206
    • Touzot, F.1    Moshous, D.2    Cros, G.3    Frange, P.4    Chornton, M.5    Friedmind, M.L.6
  • 90
    • 84896738619 scopus 로고    scopus 로고
    • B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients
    • I. Brigida, A.V. Sauer, F. Ferrua, S. Giannelli, S. Scaramuzza, V. Pistoia, and et al. B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients J Allergy Clin Immunol 133 2014 799 806
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 799-806
    • Brigida, I.1    Sauer, A.V.2    Ferrua, F.3    Giannelli, S.4    Scaramuzza, S.5    Pistoia, V.6
  • 91
    • 84897389322 scopus 로고    scopus 로고
    • Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome
    • N.P. Van Til, R. Sarwari, T.P. Visser, J. Hauer, C. Lagresle-Peyrou, G. van der Velden, and et al. Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome J Allergy Clin Immunol 133 2014 1116 1123
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1116-1123
    • Van Til, N.P.1    Sarwari, R.2    Visser, T.P.3    Hauer, J.4    Lagresle-Peyrou, C.5    Van Der Velden, G.6
  • 93
    • 84891735723 scopus 로고    scopus 로고
    • Intravenous immunoglobulin induces a functional silencing program similar to anergy in human B cells
    • J.F. Seite, C. Goutsmedt, P. Younoi, J.O. Pers, and S. Hillion Intravenous immunoglobulin induces a functional silencing program similar to anergy in human B cells J Allergy Clin Immunol 133 2014 181 188
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 181-188
    • Seite, J.F.1    Goutsmedt, C.2    Younoi, P.3    Pers, J.O.4    Hillion, S.5
  • 94
    • 84896692591 scopus 로고    scopus 로고
    • Dendritic cell immunoreceptor: A novel receptor for intravenous immunoglobulin mediates induction of regulatory T cells
    • A.H. Massoud, M. Yona, D. Xue, F. Chouiali, H. Alturaihi, A. Ablona, and et al. Dendritic cell immunoreceptor: a novel receptor for intravenous immunoglobulin mediates induction of regulatory T cells J Allergy Clin Immunol 133 2014 853 863
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 853-863
    • Massoud, A.H.1    Yona, M.2    Xue, D.3    Chouiali, F.4    Alturaihi, H.5    Ablona, A.6
  • 95
    • 84897458695 scopus 로고    scopus 로고
    • Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts
    • W.T. Shearer, T.A. Fleisher, R.H. Buckley, Z. Ballas, M. Ballow, M. Blaese, and et al. Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts J Allergy Clin Immunol 133 2014 961 966
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 961-966
    • Shearer, W.T.1    Fleisher, T.A.2    Buckley, R.H.3    Ballas, Z.4    Ballow, M.5    Blaese, M.6
  • 96
    • 84897136937 scopus 로고    scopus 로고
    • BCG vaccination in patients with severe combined immunodeficiency: Complications, risks and vaccination policies
    • B.E. Marciano, C.Y. Huang, G. Joshi, N. Rezaei, B. Costa Carvalho, Z. Allwood, and et al. BCG vaccination in patients with severe combined immunodeficiency: complications, risks and vaccination policies J Allergy Clin Immunol 133 2014 1134 1141
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1134-1141
    • Marciano, B.E.1    Huang, C.Y.2    Joshi, G.3    Rezaei, N.4    Costa Carvalho, B.5    Allwood, Z.6
  • 97
    • 84899645392 scopus 로고    scopus 로고
    • Beneficial IFN-α treatment of tumorous blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency
    • C. Papan, B. Hagel, V. Heinz, M.H. Albert, O. Ebert, J. Savalle-Belhoradsky, and et al. Beneficial IFN-α treatment of tumorous blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency J Allergy Clin Immunol 133 2014 1456 1458
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1456-1458
    • Papan, C.1    Hagel, B.2    Heinz, V.3    Albert, M.H.4    Ebert, O.5    Savalle-Belhoradsky, J.6
  • 98
    • 84901807538 scopus 로고    scopus 로고
    • Plasmacytoid dendritic cell depletion in DOCK8 deficiency: Rescue of severe herpetic infections with IFN-α2b therapy
    • S. Keles, H.H. Jabara, I. Reisli, D.R. McDonald, I. Barlan, R. Hann-Wakim, and et al. Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-α2b therapy J Allergy Clin Immunol 133 2014 1753 1755
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 1753-1755
    • Keles, S.1    Jabara, H.H.2    Reisli, I.3    McDonald, D.R.4    Barlan, I.5    Hann-Wakim, R.6
  • 99
    • 84914155258 scopus 로고    scopus 로고
    • Neutrophils in antiretroviral therapy controlled HIV demonstrate hyperactivation associated with a specific IL-17/IL-22 environment
    • L. Campillo-Gimenez, S. Casulli, Y. Dudoit, S. Seang, G. Carcelain, S. Lambert-Niclot, and et al. Neutrophils in antiretroviral therapy controlled HIV demonstrate hyperactivation associated with a specific IL-17/IL-22 environment J Allergy Clin Immunol 134 2014 1142 1152
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 1142-1152
    • Campillo-Gimenez, L.1    Casulli, S.2    Dudoit, Y.3    Seang, S.4    Carcelain, G.5    Lambert-Niclot, S.6
  • 100
    • 84895057775 scopus 로고    scopus 로고
    • Premature immune senescence during HIV-1 vertical infection relates with response to influenza vaccination
    • A. Cagigi, S. Rinaldi, A. Di Martino, E.C. Manno, P. Zangari, A. Aquilani, and et al. Premature immune senescence during HIV-1 vertical infection relates with response to influenza vaccination J Allergy Clin Immunol 133 2014 592 594
    • (2014) J Allergy Clin Immunol , vol.133 , pp. 592-594
    • Cagigi, A.1    Rinaldi, S.2    Di Martino, A.3    Manno, E.C.4    Zangari, P.5    Aquilani, A.6
  • 102
    • 84903615913 scopus 로고    scopus 로고
    • Recent developments in the search for a cure for HIV-1 infection: Targeting the latent reservoir for HIV-1
    • J.D. Siciliano, and R.F. Siciliano Recent developments in the search for a cure for HIV-1 infection: targeting the latent reservoir for HIV-1 J Allergy Clin Immunol 134 2014 12 19
    • (2014) J Allergy Clin Immunol , vol.134 , pp. 12-19
    • Siciliano, J.D.1    Siciliano, R.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.