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Abnormal antibody responses in patients with persistent generalized lymphadenopathy
H D Ochs1, A K Junker, A C Collier
1Department of Pediatrics, School of Medicine, University of Washington, Seattle 98195.
Persistent, generalized lymphadenopathy (PGL) in human immunodeficiency virus (HIV) infection impairs B and T cell function, leading to reduced antibody responses. Despite immune deficiencies, some patients remained clinically stable over three years.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Persistent, generalized lymphadenopathy (PGL) is a clinical manifestation of human immunodeficiency virus (HIV) infection.
- Understanding the impact of PGL on immune function is crucial for managing HIV.
Observation:
- Longitudinal studies assessed B and T cell function in seven homosexual men with HIV and PGL.
- Immune responses were evaluated using T-dependent and T-independent antigens, as well as recall antigens.
Findings:
- Patients with PGL exhibited abnormal antibody-mediated immunity, including lower antibody titers and impaired immunologic memory.
- A failure to switch from IgM- to IgG-isotype antibodies was observed post-immunization.
- In vitro antibody production was diminished, with some patients showing reduced mitogen responses.
Implications:
- A correlation exists between the severity of immune compromise and clinical condition in HIV-PGL patients.
- Despite significant immunologic impairment, a subset of patients remained clinically stable for up to three years.
- These findings highlight the complex interplay between immune status and clinical progression in HIV infection.
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