Neutrophil Antibody Specificity in Different Types of Childhood Autoimmune Neutropenia
- 1 September 1999
- journal article
- Published by American Society of Hematology in Blood
- Vol. 94 (5) , 1797-1802
- https://doi.org/10.1182/blood.v94.5.1797
Abstract
Autoimmune neutropenia (AIN) in children can be divided into 2 forms. In primary AIN, neutropenia is the sole abnormality, and although neutrophil counts are generally below 500 μL−1, mild bacterial infections occur. Primary AIN is mostly seen in young children and shows a self-limited course. AIN occurring in association with autoimmune diseases (secondary AIN) often shows more severe infectious complications. We analyzed clinical and serological data from 28 pediatric patients with AIN to evaluate whether there is a possible relationship between specificity of the neutrophil autoantibodies and the clinical course of the disease. Specificity of the circulating antibodies was determined with the indirect granulocyte immunofluorescence test (GIFT) and a panel of phenotyped donor neutrophils. The samples were further analyzed in the monoclonal antibody immobilization of granulocyte antigens assay (MAIGA) for neutrophil antigen (NA)1, NA2, CD11a, and CD11b specificity. With the indirect GIFT, an antibody specificity was deduced in 26 of the 28 analyzed samples. In all but 3 sera from patients with primary AIN, NA1-(76%) or NA2-(10%) specific antibodies were detected with the indirect GIFT. In 2 samples, the reactivity in the indirect GIFT was too weak to draw conclusions, but the MAIGA showed NA1 and/or NA2 specificity of the antibodies. One serum, from a patient with primary AIN with a persistent neutropenia for more than 6 years, contained NA1, possibly pan-FcγRIIIb, and CD11a antibodies. In 4 sera from patients with primary AIN, weak antibodies with CD11a or CD11b specificity were detected with the MAIGA. Sera from 7 patients with secondary AIN contained in all cases antibodies with pan-FcγRIIIb specificity, as deduced from the indirect GIFT results and absorbance/elution experiments performed with 2 sera. The MAIGA confirmed this for only 1 of the 5 tested sera. Furthermore, CD11a antibodies were detected in 1 of the 5 tested sera. In conclusion, our results indicate that primary AIN is usually associated with NA-specific antibodies, whereas secondary AIN seems to be associated with pan-FcγRIIIb antibodies. Thus, characterization of the antibodies in sera from children with AIN discriminates patients with primary AIN from those with secondary AIN.Keywords
This publication has 15 references indexed in Scilit:
- Report on the second international granulocyte serology workshopTransfusion, 1997
- Characterization of a New Alloantigen (SH) on the Human Neutrophil Fcγreceptor IIIbBlood, 1997
- The use of rh‐G‐CSF in chronic autoimmune neutropenia: reversal of autoimmune phenomena, a case historyBritish Journal of Haematology, 1996
- Chronic neutropenia of childhood: frequent association with parvovirus infection and correlations with bone marrow culture studiesBritish Journal of Haematology, 1993
- Analysis of granulocyte‐reactive antibodies using an immunoassay based upon monoclonal‐antibody‐specific immobilization of granulocyte antigensTransfusion Medicine, 1993
- Autoimmune neutropenia: clinical and laboratory studies in 143 patientsAnnals of Hematology, 1991
- Autoimmunization against the neutrophil-specific NA1 antigen is associated with HLA-DR2Human Immunology, 1991
- Autoimmune neutropenia of infancyThe Journal of Pediatrics, 1986
- Elution of Granulocyte and Platelet AntibodiesVox Sanguinis, 1982
- Chronic Autoimmune Neutropenia Due to Anti-NA2 AntibodyNew England Journal of Medicine, 1975