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In Vitro Assay to Evaluate the Impact of Immunoregulatory Pathways on HIV-specific CD4 T Cell Effector Function
Published on: October 16, 2013
Immunologic evaluation of persons infected with human immunodeficiency virus
1AIDS Program, Centers for Disease Control, Atlanta, Georgia.
Insights
HIV infection severely impacts immunity, decreasing CD4+ helper and CD8+ suppressor T cells. Immune testing, including T-cell counts and immunoglobulin levels, helps assess HIV-related immunosuppression and guide treatment.
Area of Science:
- Immunology
- Virology
- Clinical Laboratory Science
Background:
- HIV infection profoundly affects cellular and humoral immunity.
- Key immune cells like CD4+ (helper) and CD8+ (suppressor) T cells are significantly reduced.
- Macrophages also exhibit functional deficits in HIV-infected individuals.
Purpose of the Study:
- To outline the immunological changes associated with HIV infection.
- To identify key laboratory tests for evaluating immune status in HIV patients.
- To discuss the prognostic value of immunological markers and future therapeutic implications.
Main Methods:
- Enumeration of circulating CD4+ and CD8+ T cells.
- Quantitation of circulating immunoglobulins.
- Assessment of T-cell proliferation in vitro and antibody responses in vivo/in vitro.
Main Results:
- HIV infection leads to decreased CD4+ and CD8+ T cell counts.
- Cellular immune function, including T-cell proliferation, is often impaired.
- Humoral immunity shows B-cell activation and diminished antibody responses.
- Macrophage functions are also frequently compromised.
Conclusions:
- CD4+ and CD8+ T cell counts and immunoglobulin levels are crucial for assessing HIV-related immunosuppression.
- These immunological tests aid in differentiating HIV from other immunodeficiencies and selecting treatments.
- Future research and therapies aim to restore normal immune function in HIV-infected individuals.
Abstract:
Persons infected with HIV show changes in all aspects of immunity. Cellular immunity is affected most markedly, with decreased numbers of CD4+ (helper) and CD8+ (suppressor) T cells. Cellular immune function in vitro is frequently abnormal, as assessed by ability of T cells to proliferate in response to antigens or mitogens. Impaired humoral immunity is manifested in polyclonal B-cell activation and in impaired antibody responses to soluble antigens in vivo and in vitro. Numerous functional defects of macrophages have also been reported. The most valuable clinical laboratory tests for evaluation of the immune status of the HIV-infected individual are enumeration of circulating CD4+ and CD8+ cells and quantitation of circulating immunoglobulins. The results of these tests can help differentiate the immunosuppression caused by HIV from other causes of immunodeficiency. Helper T-cell counts are also important for selecting appropriate treatment regimens. Combinations of the results of these tests with those of virus culture or antigen detection assays provide additional prognostic information. Future research may help us recognize other patterns of immunodeficiency with specific clinical implications. It is hoped that new therapies, both antiviral and immune reconstitutive, will soon become available; at such time immunologic testing will be able to chart the return to normal immune function.
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