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Role of Th17 T‐Lymphocytes in Advanced AIDS Patients with Marked CD4+ T Cell Depletion
Author(s) -
Singleterry Will Landry,
Lewis Robert E.,
Bigler Steven,
Cruse Julius M.
Publication year - 2011
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.25.1_supplement.614.20
In the final stages of an HIV infection (AIDS), the human immune system is unable to produce an effective response due to severe depletion of CD4+ T cells. Our preliminary research indicates that though there is CD4+ T cell depletion, the Th17 T‐cells, as a percentage of the T cell population, increase in the final stages of AIDS. Peripheral blood samples from 23 different patients with AIDS (CD4+ T cell count below 200/μL) were measured using flow cytometry. In humans, the classic Th17 T cell falls within a CD161+ subgroup, and are also positive for CD3, CD4 and CCR6. In our 6 healthy controls, the Th17 T cell population as a percentage of the CD161 subgroup had a mean of 0.16% of the CD161 population. Of those AIDS patients with a CD4+ T cell count below 20 (n=12), the mean Th17 T cell population of the CD161 subgroup was 13.99%. In AIDS patients with CD4+ T cell count below 10 (n=8), the mean Th17 T cell population of the CD161 subgroup was 20.01%. Our hypothesis is that the altered immune state in AIDS induces the differentiation of Th17 T cells from those remaining naïve T cells in order to repel the opportunistic infections occurring in these patients. However, due to a lack of Th1 T cells to transition from the Th17 response, the body attempts to increase that initial physiologic inflammatory response by differentiating more Th17 T cells.

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