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Elevated KIR expression and diminished intensity of CD7 on NK cell subsets among treatment naïve HIV infected Ethiopians. | LitMetric

AI Article Synopsis

  • Natural killer (NK) cells play a vital role in the body's initial defense against viral infections like HIV, through their ability to kill infected cells and produce antiviral cytokines.
  • Researchers studied 15 HIV patients and 16 healthy individuals to compare NK cell subsets and their markers using flow cytometry, finding that specific NK cell subsets were less frequent in HIV patients.
  • The study revealed notable differences in NK cell markers, such as lower CD7 levels and increased KIR3DL1/S1 cells among certain NK cell populations in HIV patients, suggesting new areas for further research.

Article Abstract

Natural killer (NK) cells are crucial effector cells of the innate immune response to viral infections, including HIV, through cytolytic activity and the production of cytokines with anti-HIV activities. We recruited 15 treatment naïve HIV patients and 16 healthy controls (HC) to assess NK cell subsets or expression of multiple markers by flow cytometry. The frequency of circulating CD56CD16 and CD56CD16 NK cell subsets was significantly lower among the HIV group than in HC. The CD56CD16 subset was higher in HIV patients, but this was only apparent when gated among total NK cells, not total lymphocytes. NK cells among HIV participants also showed a lower and higher frequency of CD8 and HLA-DR expressing cells, respectively. In addition, CD7 median fluorescent intensity and CD2CD7 frequencies were significantly lower in HIV patients. A distinct population of KIR3DL1/S1 cells was unexpectedly higher among CD56CD16 NK cells in HIV patients. In conclusion, this study in the Ethiopian setting confirms many previous findings, but the down-regulation of CD7 and enhanced KIR3DL1/S1 within the CD56 subsets have not been widely reported among HIV patients and merit further research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427747PMC
http://dx.doi.org/10.1038/s41598-022-18413-3DOI Listing

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