Lymph node pathology in primary combined immunodeficiency diseases

Springer Seminars in Immunopathology

Volumn 19, Issue 4, 1998, Pages 459-478

  Facchetti, Fabio ^a   Blanzuoli, Laura ^a   Ungari, Marco ^a   Alebardi, Olga ^a   Vermi, William ^a  

^a UNIVERSITY OF BRESCIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

COMBINED IMMUNODEFICIENCY; CONTROLLED STUDY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNE DEFICIENCY; LYMPH NODE; LYMPHOCYTE; PATHOLOGY; PHENOTYPE; PRIORITY JOURNAL; REVIEW; WISKOTT ALDRICH SYNDROME;

B-LYMPHOCYTES; FEMALE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; LYMPH NODES; MALE; T-LYMPHOCYTES;

EID: 0031942450     PISSN: 03444325     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF00792602     Document Type: Review

References (75)

1. Bahadoran P, Rieux-Laucat F, Canioni D, Le Diest F, Fischer A, Brousse N (1996) Significance of interdigitating reticulum cells in Omenn's syndrome. Am J Surg Pathol 20 : 1032
2. Bruton OC (1952) Agammaglobulinemia. Pediatrics 9 : 722
3. Buckley RH, Schiff RI, Schiff SE, Markett LM, Williams LW, Harville TO, Roberts JL, Puck JM (1997) Human severe combined immunodeficiency: genetic, phenotipic, and functional diversity in one hundred eight infants. J Pediatr 130 : 378
4. Businco L, Di Fazio A, Ziruolo MG, Boner AL, Valletta EA, Ruco LP, Vitolo D, Ensoli B, Paganelli R (1987) Clinical and immunological findings in four infants with Omenn's syndrome: a form of severe combined immunodeficiency with phenotypically normal T cells, elevated IgE, and eosinophilia. Clin Immunol Immunopathol 44 : 123
5. Cao X, Shores EW, Hu-Li J, Anver MR, Kelsall BL, Russel SM, Drago J, Noguchi M, Grinberg A, Bloom ET, Paul PE, Katz SI, Love PE, Leonard WJ (1995) Defective lymphoid development in mice lacking expression of the common cytokine receptor chain. Immunity 2 : 223
6. Castenholz, A (1990) Architecture of the lymph node with regard to its function. In: Grundmann E, Vollmer E (eds) Reaction patterns of the lymph node. Part 1. Cell types and functions. Springer, Berlin Heidelberg New York, pp 1-32
7. +TNFα. J Exp Med 184 : 695
8. Chilosi M, Facchetti F, Notarangelo LD, Romagnani S, Del Prete G, Almerigogna F, De Carli M, Pizzolo G (1996) CD30 cell expression and abnormal soluble CD30 serum accumulation in Omenn's syndrome: evidence for a T helper 2-mediated condition. Eur J Immunol 26 : 329
9. Conley ME (1985) B cells in patients with X-linked agammaglobulinemia. J Immunol 134 : 3070
10. Cottier H, Turk J, Sobin L (1973) A proposal for a standardized system of reporting human lymph node morphology in relation to immunological function. J Clin Pathol 26 : 317
11. Cottier H, Kraft R, Meister F (1990) Primary immunodeficiency syndromes and their manifestations in lymph nodes. In: Grundmann E, Vollmer E (eds) Reaction patterns of the lymph node. Part 2. Reactions associated with neoplasia and immune deficient states. Springer, Berlin Heidelberg New York, pp 81-155
12. De Bruyn PPH, Cho Y (1990) Structure and function of high endothelial postcapillary venules in lymphocyte circulation. In: Grundmann E, Vollmer E (eds) Reaction patterns of the lymph node. Part 1. Cell types and functions. Springer, Berlin Heidelberg New York, pp 85-101
13. Deny JMJ, Ochs HD, Francke U (1994) Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 78 : 635
14. De Saint-Basile G, Le Diest F, Villartay JP de, Cerf-Bernussan N, Joumet O, Brousse N, Griscelli C, Fischer A (1991) Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome). J Clin Invest 87 : 1352
15. De Wolf-Peeters C, Delabie J (1993) Anatomy and histopathology of lymphoid tissue. Semin Oncol 20 : 555
16. Donner M, Schwartz M, Carlsson KU, Holmberg L (1988) Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome. Blood 72 : 1849
17. Elenitoba-Johnson KSJ, Jaffe ES (1997) Lymphoproliferative disorders associated with congenital immunodeficiencies. Semin Diagn Pathol 14 : 35
18. Emile JF, Durandy A, Le Deist F, Fischer A, Brousse N (1997) Epidermal Langerhans' cells in children with primary T-cell immune deficiencies. J Pathol 183 : 70
19. Facchetti F, De Wolf-Peeters C, Van den Oord JJ, De Vos R, Desmet VJ (1988) Plasmacytoid T cells: a cell population normally present in the reactive lymph node. An immunohistochemical and electronmicroscopic study. Hum Pathol 19 : 1085
20. Facchetti F, De Wolf-Peeters C, Van den Oord JJ, Meijer CJLM, Pals ST, Desmet VJ (1989) Anti-high endothelial venule monoclonal antibody HECA-452 recognizes plasmacytoid T cells and delineates an "extranodular" compartment in the reactive lymph node. Immunol Lett 20 : 277
21. Facchetti F, Appiani C, Salvi L, Levy J, Notarangelo LD (1995) Immunohistologic analysis of ineffective CD40-CD40 ligand interaction in lymphoid tissues from patients with X-linked immunodeficiency with Hyper-IgM. J Immunol 154 : 6624
22. Facchetti F, Blanzuoli L, Vermi W, Notarangelo LD, Giliani S, Fiorini M, Fasth A, Stewart DM, Nelson DL (in press) Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome. J Pathol
23. Filipovich AH, Mathur A, Kamat D, Kersey JH, Shapiro RS (1994) Lymphoproliferative disorders and other tumors complicating immunodeficiencies. Immunodeficiency 5 : 91
24. Fischer A (1993) Primary T cell immudeficiencies. Curr Opin Immunol 5 : 569
25. Fossum SW, Ford WL (1985) The organization of cell populations wityhin lymph nodes: their origin, life history and functional relationships. Histopathology 9 : 469
26. Gallego MD, Santamaria M, Peña J, Molina IJ (1997) Defective actin reorganization and polymerization of Wiskott-Aldrich T cells in response to CD3-mediated stimulation. Blood 90 : 3089
27. Gosseye S, Diebold N, Griscelli C, Nezelof C (1983) Severe combined immunodeficiency disease: a pathological analysis of 26 cases. Clin Immunol Immunopathol 29 : 58
28. Heymer B, Niethammer D, Spanel M, Galle J, Kleihauer E, Haferkamp E (1977) Pathomorphology of humoral, cellular and combined primary immunodeficiencies. Virchows Arch [A] 374 : 87
29. Huber J, Zegers BJM, Schuurman HJ (1992) Pathology of congenital immunodeficiencies. Semin Diagn Pathol 9 : 31
30. Jouan H, Le Deist F, Nezelof C (1987) Omenn's syndrome - Pathologic arguments in favor of a graft versus host pathogenesis: a report of nine cases. Hum Pathol 18 : 1101
31. Kawai T, Kawano K (1973) Immunopathology of primary immunodeficiency diseases. Acta Pathol Jpn 23 : 887
32. Korthäuer U, Graf D, Mages HW, Brière F, Padayachee M, Malcolm S, Ugazzio AG, Notarangelo LD, Levinsky RJ, Kroczek RA (1993) Defective expression of T cell CD40 ligand causes X-linked immunodeficiency with hyper IgM. Nature 361 : 539
33. +, Vβ3 expressing, cytotoxic T lymphocytes in the peripheral blood. J Immunol 149 : 3403
34. Lonsdale D, Deodhar SD, Mercer RD (1967) Familial granulocytopenia and associated immunoglobulin abnormality. J Pediatr 71 : 790
35. Luscieti P, Hubschmid T, Cottier H, Hess MV, Sobin LH (1980) Human lymph node morphology as a function of age and site. J Clin Pathol 33 : 454
36. Macchi P, Villa A, Giliani S, Sacco MG, Frattini A, Porta F, Ugazio AG, Johnson JA, Candotti F, O'Shea JJ, Vezzoni P, Notarangelo LD (1995) Mutation of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID). Nature 377 : 65
37. + T cell clones in human immunodeficiency virus infection. J Exp Med 180 : 2407
38. Markert ML (1993) Purine nucleoside phosphorylase. In: Rosen FS, Seligmann M (eds) Immunodeficiencies. Harvood Academic, Chur, pp 197-224
39. Martin JV, Willoughby PB, Giusti V, Price G, Cerezo L (1995) The lymph node pathology of Omenn's syndrome. Am J Surg Pathol 19 : 1082
40. Moreno LA, Gottrand F, Turck D, Monouvrier-Hanu S, Mazingue F, Morisot C, Le Deist F, Ricour C, Nihoul-Feketé C, Debeugny P, Griscelli C, Farriaux JP (1990) Severe combined immunodeficiency syndrome associated with autosomal recessive familial multiple gastrointestinal atresias: study of a family. Am J Med Genet 37 : 143
41. Noguchi M, Yi H, Rosenblatt HM, Filipovich AH, Adelstein S, Modi WS, McBride OW, Leonard WJ (1993) Interleukin-2 receptor γ chain mutation results in X-linked severe combined immunodeficiency in humans. Cell 73 : 147
42. Nonoyama S, Hollenbaugh D, Aruffo A, Ledbetter JA, Ochs HD (1993) B cell activation via CD40 is required for specific antibody production by antigen-stimulated human B cells. J Exp Med 178 : 1097
43. Notarangelo LD, Duse M, Ugazio AG (1992) Immunodeficiency with hyper-IgM (HIM). Immunodefic Rev 3 : 101
44. Ochs HD, Davis SD, Mickelson E, Lerner KG, Wedgwood RJ (1974) Combined immunodeficiency and reticuloendotheliosis with eosinophilia. J Pediatr 85 : 463
45. Omenn GS (1965) Familial reticuloendotheliosis with eosinophilia. N Engl J Med 273 : 427
46. Park SY, Saijo K, Takahashi T, Osawa M, Arase H, Hirayama N, Miyake K, Nakauchi H, Shirasawa T, Saito T (1995) Developmental defects of lymphoid cells in Jak3 kinase-deficient mice. Immunity 3 : 771
47. Parott DMV, Sousa MAB de (1966) Changes in the thymus dependent areas of lymph nodes after immunological stimulation. Nature 212 : 1316
48. Perez-Atayde AR, Rosen FS (1995) Pathology of the primary immunodeficiency disease. In: Colvin RB, McCluskey (eds) Diagnostic immunopathology. Raven Press, New York, pp 241-259
49. Ratech H, Hirshhorn R, Greco MA (1989) Pathologic findings in adenosine deaminase deficient-severe combined immunodeficiency. Thymus, spleen, lymph node, and gastrointestinal tract lymphoid tissue alterations. Am J Pathol 135 : 1145
50. Remold-O'Donnel E, Colley J, Shcherbina A, Hagemann TL, Kwan SP, Kenney DM, Rosen FS (1997) Variable expression of WASP in B cell lines of Wiskott-Aldrich syndrome patients. J Immunol 158 : 4021
51. Renshaw BR, Fanslow WC III, Armitage RJ, Kampbell KA, Liggit D, Wright B, Davison BL, Maliszewski CR (1994) Humoral immune responses in CD40 ligand-deficient mice. J Exp Med 180 : 1889
52. Resta R, Thompson LF (1997) SCID: the role of adenosine deaminase deficiency. Immunol Today 18 : 371
53. Rosen FS, Wedgwood RJP, Eibl M, et al. (1997) Primary immunodeficiency diseases. Report of a WHO scientific group. Clin Exp Immunol 109(s) : 1
54. + lymphocyte population in the blood of SIV-infected macaque is not reflected in lymph nodes. AIDS Res Hum Retroviruses 9 : 639
55. Resok BI, Bostad L, Voltervik P, Bjerknes R, Olofsson J, Asjo B, Brinchmann JE (1996) Reduced CD4 cell counts in blood do not reflect CD4 cell depletion in tonsillar tissue in asymptomatic HIV-1 infection. AIDS 10 : F35
56. Rothenberg ME, White FV, Chilmonczyk B, Chatila T (1995) A syndrome involving immunodeficiency and multiple intestinal atresias. Immunodeficiency 5 : 171
57. + Langerhans-like cells. Virchows Arch [A] 407 : 69
58. Sander CA, Medeiros LJ, Weiss LM, Yano T, Sneller MC, Jaffe ES (1992) Lymphoproliferative lesions in patients with common variable immunodeficiency syndrome. Am J Surg Pathol 16 : 1170
59. Saunders D, Lucas K, Ismaili J, Wu L, Maraskovsky E, Dunn E, Shortman K (1996) Dendritic cell development in culture from thymic precursor cells in the absence of granulocyte-macrophage colony stimulating factor. J Exp Med 184 : 2185
60. Snover DC, Frizzera G, Spector BD, Perry GS, Kersey JH (1981) Wiskott-Aldrich syndrome: histopathologic findings in the lymph nodes and spleens of 15 patients. Hum Pathol 12 : 821
61. Stekel DJ, Parker CE, Nowak MA (1997) A model of lymphocyte recirculation. Immunol Today 18 : 216
62. Stephan JL, Vlekova V, Le Deist F, Blanche S, Donadieu J, De Saint Basile G, Durandy A, Griscelli C, Fisher A (1993) Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients. J Pediatr 123 : 564
63. Stewart DM, Treiber-Held S, Kurman CC, Facchetti F, Notarangelo LD, Nelson DL (1996) Studies of the expression of the Wiskott-Aldrich syndrome protein. J Clin Invest 97 : 2627
64. + bone marrow precursors cultured witch-kit-ligand, GM-CSF, and TNF. J Immunol 154 : 5851
65. Tachinami T, Koizumi S, Yachic A, Yamagami M, Yokoi T, Ohno I, Taniguchi N, Takada I, Kawashima A, Okada Y (1990) Immune status in two brothers with Omenn's syndrome: no discernible chimerism on FACS analysis using a monoclonal antibody specific for a maternally restricted HLA antigen. Am J Pediatr Hematol Oncol 12 : 343
66. Timens W, Boes A, Rozeboom-Uiterwijk T, Poppema S (1988) Immuno-architecture of human fetal lymphoid tissues. Virchows Arch [A] 413 : 563
67. Ugazio AG, Duse M, Notarangelo LD, Plebani A, Porta F (1994) Il bambino immunodepresso. Casa Editrice Ambrosiana, Milano
68. Van der Valk P, Meijer CJLM (1987) The histology of reactive lymph nodes. Am J Surg Pathol 11 : 866.
69. Van den Oord JJ, Facchetti F, Delabie J, Wolf-Peeters C de (1990) T lymphocytes in non-neoplastic lymph nodes. In: Grundmann E, Vollmer E (eds) Reaction patterns of the lymph node. Part 1. Cell types and functions. Springer, Berlin Heidelberg New York, pp 149-178
70. Walker MW, Lovell MA, Kelly TE, Golden W, Saulsbury FT (1993) Multiple areas of intestinal atresia associated with immunodeciency and posttransfusion graft-versus-host disease. J Pediatr 123 : 93
71. Wiskott A (1937) Familiarer, angeborener Morbus Werlhofiì? Monatschr Kinderheilk 68 : 212
72. Wolf U (1997) Identical mutations and phenotypic variations. Hum Genet 100 : 305
73. Xu J, Foy TM, Laman JD, Elliott EA, Dunn JJ, Waldschmidt TJ, Elsemore J, Noelle RJ, Flavell RA (1994) Mice deficient for the CD40 ligand. Immunity 1 : 423
74. Zhu Q, Zhang M, Blaese RM, Derry JMJ, Junker A, Francke U, Chen SH, Ochs HD (1995) The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutation of the same gene. Blood 86 : 3797
75. Zhu Q, Watanabe C, Liu T, Hollenbaugh D, Blaese MR, Kanner SB, Aruffo A, Ochs HD (1997) Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype. Blood 90 : 2680