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B-cell reactivity in homosexuals with persistent generalized lymphadenopathy (PGL)
1Department of Internal Medicine, Christian Albrecht University, Kiel, Federal Republic of Germany.
Summary
Early B-cell dysfunction occurs in individuals with persistent generalized lymphadenopathy (PGL) and Human Immunodeficiency Virus (HIV) infection, independent of T-cell defects. This immune imbalance is similar to that seen in Acquired Immunodeficiency Syndrome (AIDS).
Area of Science:
- Immunology
- Virology
- Cell Biology
Background:
- Acquired Immunodeficiency Syndrome (AIDS) is characterized by T-cell dysfunction.
- Hypergammaglobulinemia and autoimmune phenomena in AIDS suggest B-cell involvement.
- Human T-lymphotropic virus type III/Lymphadenopathy-associated virus (HTLV-III/LAV) infection may cause T-cell-independent B-cell abnormalities.
Purpose of the Study:
- To investigate early B-cell dysfunctions in a high-risk group for AIDS.
- To compare B-cell responses in patients with Persistent Generalized Lymphadenopathy (PGL) to those with AIDS/AIDS-Related Complex (ARC) and healthy controls.
Main Methods:
- Examined six homosexual men with PGL and HTLV-III/LAV antibodies.
- Conducted in vitro studies on B-cell proliferation using 3H-thymidine uptake.
- Assessed B-cell differentiation by measuring immunoglobulin secretion in response to polyclonal B-cell activators (PBAs).
Main Results:
- Profound alterations in both B-cell proliferation and differentiation responses were observed in the PGL group.
- A weak B-cell response to T-cell-independent PBAs was noted.
- These B-cell dysfunctions in PGL patients were similar to those found in AIDS patients.
Conclusions:
- B-cell dysfunction in PGL patients is not solely due to T-cell defects.
- Early B-cell abnormalities are present in individuals at high risk for AIDS.
- Findings suggest a significant role for intrinsic B-cell defects in HIV infection pathogenesis.

