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Published on: August 31, 2014
IgA immunity in HIV type 1-infected chimpanzees. I. Systemic immunity
K P Black1, P N Fultz, M Girard
1Department of Microbiology, University of Alabama at Birmingham, 35294-2170, USA.
Human immunodeficiency virus (HIV) infection in chimpanzees can cause abnormalities in immunoglobulin A (IgA) levels, similar to those seen in humans. This study investigated these changes and found specific IgA subclass alterations and enhanced IgA reactivity against HIV antigens in infected chimpanzees.
Area of Science:
- Immunology
- Virology
- Primatology
Background:
- Human immunodeficiency virus (HIV) infection disrupts cellular and humoral immunity, notably affecting B lymphocyte function and immunoglobulin A (IgA) regulation in humans.
- Elevated serum IgA concentrations are a common observation in HIV-infected individuals, indicating immune system dysregulation.
Purpose of the Study:
- To investigate whether HIV-1 infection induces similar IgA abnormalities in chimpanzees as observed in humans.
- To analyze changes in total IgA, IgG, and IgM levels and specific antibody responses to HIV antigens in infected chimpanzees.
Main Methods:
- Longitudinal serum sampling from six HIV-1-infected chimpanzees and one control.
- Quantification of total IgA, IgG, and IgM levels.
- ELISA for IgA subclasses, enzyme immunoassay (EIA), and Western blot analysis for HIV-specific antibodies (IgG, IgA, IgA1, IgA2), including analysis of IgG-depleted sera.
Main Results:
- Two infected chimpanzees showed increased serum immunoglobulins, while two others exhibited a transient decrease in IgA, IgG, and IgM.
- Two chimpanzees displayed stable immunoglobulin levels throughout the study period.
- Abnormalities in the IgA2 subclass were noted in animals without significant overall immunoglobulin fluctuations; IgA reactivity against HIV antigens was sometimes enhanced after IgG depletion.
Conclusions:
- HIV-1 infection can induce serum IgA abnormalities in chimpanzees, mirroring some human responses.
- Findings contribute to understanding HIV-induced humoral immune responses and may inform research on HIV in humans.
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