Spontaneous release of interferon as a predictor of clinical evolution in HIV-positive subjects
Infection, ISSN: 0300-8126, Vol: 19, Issue: 1, Page: 7-12
1991
- 2Citations
- 3Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Article Description
In order to establish a correlation with disease progression we prospectively evaluated ten clinical and immunologic parameters in 102 consecutive HIV-positive subjects. The eight immunologic variables were:in vitro spontaneous interferon release by peripheral blood monocytic cells, alpha- and gamma-interferon production induced by Newcastle Disease Virus and PHA, Multitest Mérieux score, PHA- and CON-A-induced lymphocyte transformation, absolute number of CD4+ cells and CD4/CD8 ratio, respectively. The two baseline clinical variables were risk factor and disease presentation. Generalized Wilcoxon analysis indicated a significant correlation of one clinical (disease presentation at entry) and three immunologic variables (spontaneous interferon release, CD4+ cell number, Multitest Mérieux) with disease progression. Baseline spontaneous release of alpha, acid-labile interferon showed the best correlation with disease progression, and appeared to be significantly associated with CD4+ cell loss. Spontaneous release of acid-labile alpha interferon by mononuclear cells in vitro could be highly predictive of disease evolution in HIV-Ab positive, AIDS-free subjects. © 1991 MMV Medizin Verlag GmbH München.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0025959444&origin=inward; http://dx.doi.org/10.1007/bf01643747; http://www.ncbi.nlm.nih.gov/pubmed/2013514; http://link.springer.com/10.1007/BF01643747; http://www.springerlink.com/index/pdf/10.1007/BF01643747; http://www.springerlink.com/index/10.1007/BF01643747; https://dx.doi.org/10.1007/bf01643747; https://link.springer.com/article/10.1007/BF01643747
Springer Science and Business Media LLC
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