Severe neutropenia associated with IgG2 subclass deficiency and bone marrow T-lymphocyte infiltration

American Journal of Hematology

Volumn 57, Issue 3, 1998, Pages 241-244

  Lassoued, K ^a   Oksenhendler, E ^a   Lambin, J P ^b   Cazals Hatem, D ^a   Clauvel, J P ^a  

^a SAINT LOUIS HOSPITAL   (France)

^b INSTITUT NATIONAL DE LA TRANSFUSION SANGUINE   (France)

Author keywords

IgG2 subclass deficiency; Immunodeficiency; Lymphoproliferation; Neutropenia

Indexed keywords

CORTICOSTEROID; CYCLOPHOSPHAMIDE; IMMUNOGLOBULIN; IMMUNOGLOBULIN G2; RECOMBINANT GRANULOCYTE COLONY STIMULATING FACTOR;

ADULT; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; DISEASE ASSOCIATION; FEMALE; HELPER CELL; HUMAN; IMMUNOGLOBULIN G DEFICIENCY; LYMPHOCYTE PROLIFERATION; LYMPHOCYTIC INFILTRATION; MALE; NEUTROPENIA; PRIORITY JOURNAL; RECURRENT INFECTION; T LYMPHOCYTE; T LYMPHOCYTE SUBPOPULATION;

ADULT; BONE MARROW; CD4-POSITIVE T-LYMPHOCYTES; CD8-POSITIVE T-LYMPHOCYTES; FATAL OUTCOME; FEMALE; HUMANS; IGG DEFICIENCY; LYMPHOCYTE ACTIVATION; MALE; MIDDLE AGED; NEUTROPENIA; POLYMERASE CHAIN REACTION;

EID: 0031909195     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(199803)57:3<241::AID-AJH12>3.0.CO;2-D     Document Type: Article

References (24)

1. Aucouturier P, Lacombe C, Brenard C, Lebranchu Y, Seligmann M, Griscelli C, Preud'homme JL: Serum IgG subclass levels in patients with primary immunodeficiency syndrome or abnormal susceptibility to infections. Clin Immunol Immunopathol 51:37, 1989.
2. Preud'homme JL, Hanson LA: IgG subclass deficiency. In Rosen FS, Seligmann M (eds): "Immunodeficiencies." Philadelphia: Harwood Academic Publishers, 1993.
3. De Gracia J, Miravitlles M, Vendrell M, Rodrigo MJ, Codina R, Morell F: IgG subclasses in patients with symptomatic IgA deficiency. Med Clin 104: 728, 1995.
4. Björkander J, Bake B, Oxelius VA, Hanson LA: Impaired lung function in patients with IgA deficiency and low levels of IgG2 or IgG3. N Engl J Med 313:720, 1985.
5. Bussel J, Morell A, Skvarill F: IgG2 deficiency in autoimmune cytopenias. In Hanson LA, Söderström T, Oxelius VA (eds): "Immunoglobulin Subclass Deficiencies." Monographs in Allergy. Basel: Karger, 1986.
6. Jimenez A, Lopez-Trascaca M, Fontan G: Incidence of selective IgG2 deficiency in patients with vascularitis. Clin Exp Immunol 78:149, 1989.
7. Duse M, Tiberti S, Plabani A, Avanzini MA, Gargenghi M, Menegati E, Monafo V, Ugazio AG: IgG2 deficiency and intractable epilepsy of childhood. In Hanson LA, Söderström T, Oxelius VA (eds): "Immunoglobulin Subclass Deficiencies." Monographs in Allergy. Basel: Karger, 1986.
8. Lambin P, Gervais A, Levy M, Defendini E, Dubarry M, Lebon P, Rouger P, Schuller E: Intrathecal Synthesis of IgG subclasses in multiple sclerosis and in acquired immunodeficiency syndrome (AIDS). J Neuroimmunol 35:179, 1991.
9. Alper CA, Johnson AM: Immunofixation electrophoresis: Technique for the study of protein polymorphism. Vox Sanguinis 17:445, 1969.
10. Ritchie RF, Smith R: Immunofixation. I. General principles and application to agarose gel electrophoresis. Clin Chem 22:497, 1976.
11. Verheugt FW, Von dem Borne AE, Decary F, Engelfriet CP: The detection of granulocyte alloantibodies with an indirect immunofluorescence test. Br J Haematol 36:533, 1977.
12. Verheugt FW, Von dem Borne AE, Van Noord-Bokhorst JC, Engelfriet CP: Auto-immune granulocytopenia: The detection of granulocyte autoantibodies with the immunofluorescence test. Br J Haematol 39:339, 1978.
13. McCullough J, Clay ME, Priest JR, Jensen NJ, Lau S, Noreen HJ, Krivit W, Lalezari PA: A comparison of methods for detecting leukocyte antibodies in auto-immune neutropenia. Transfusion 21:483, 1981.
14. Gratas C, Menot ML, Dresch C, Chomienne C: Retinoid acid supports granulocytic but not erythroid differentiation of myeloid progenitors in normal bone marrow cells. Leukemia 7:1156, 1993.
15. Baruchel A, Cayuela JM, Mac Intyre E, Beyer R, Sigaux F: Assessment of clonal evolution at Ig/TCR loci in acute lymphoblastic leukemia by single strand conformation polymorphism studies and highly resolutive PCR derived methods: Implication for several strategies of minimal residual disease detection. Br J Haematol 90:85, 1995.
16. De Gracia J, Rodrigo MJ, Morell F, Vendrell M, Miravittles M, Cruz MJ, Codina R, Bofill JM: Am J Respir Crit Care Med 153:650, 1996.
17. Hermaszewski RA, Webster ADB: Primary hypogammaglobulinemia: A survey of clinical manifestations and complications. Q J Med 86:31, 1993.
18. Fillipovich AH, Mathur A, Kamat D, Kersey JH, Shapiro RS: Lymphoproliferative disorders and other tumors complicating immunodeficiencies. Immunodeficiency 5:91, 1994.
19. Benkerrou M, Gougeon ML, Griscelli C, Fischer A: Hypogammaglobulinémie G et A avec hypergammaglobulinémie M. A propos de 12 observations. Arch Fr Pediatr 47:345, 1990.
20. Cunningham-Rundles C, Lieberman P, Hellman G, Chaganti RS: Non Hodgkin's lymphoma in common variai immunodeficiency. Am J Haematol 37:65, 1991.
21. Sanders CA, Medeiros LJ, Weiss LM, Yano T, Snaller MC, Jaffe ES: Lymphoproliferative lesions in patients with common variable immunodeficiency syndrome. Am J Surg Pathol 16:1170, 1992.
22. Notarangelo LD, Duse M, Ugazio AG: Immunodeficiency with hyper-IgM (HIM). In Rosen FS, Seligmann M (eds): "Immunodeficiencies." Philadelphia: Harwood Academic Publishers, 1993.
23. Paller AS: Immunodeficiency syndromes: X-linked agammaglobulinemia, common variable immunodeficiency, Chediak Higashi syndrome, Wiskott-Aldrich syndrome and X-linked lymphoproliferative disorder. Dermatol Clin 13:65, 1995.
24. Ferrero D, Pregno P, Omedè P, Dianzani U, Carbone A, Francia Di Celle P, Gallo E: Cyclic neutropenia and severe hypogammaglobulinemia in a patient with excess of CD8-positive T lymphocytes: Response to G-CSF therapy. Haematologica 78:49, 1993.