P169 Association between CXCR4 and TRAIL pathway expression in CD4 T lymphocytes from HIV+ ART-naïve patients. (14th July 2019)

• Record Type: Journal Article
• Authors: Ratkovich-Gonzalez, Sarah; Jimenez, Judith De Arcos; Gonzalez-Hernandez, Luz; Andrade-Villanueva, Jaime; Alvarez-Zavala, Monserrat; Sanchez-Reyes, Karina
• Is Part Of: Sexually transmitted infections. Volume 95(2019)Supplement 1
• Page Start: A129
• Page End: A130
• Publication Date: 2019-07-14
• Subjects: HIV -- immunity; Sexually transmitted diseases -- Periodicals; HIV infections -- Periodicals; 616.951005
• DOI: 10.1136/sextrans-2019-sti.328
• Languages: English
• ISSNs: 1368-4973

Abstract

Abstract : Background: HIV infection is characterized by immune cells depletion, apoptosis is one of the main mechanisms described. It has been reported that, the union of HIV to coreceptor CXCR4 can induce Fas independent apoptosis on T cells. In a few in vitro studies it has been proved that stimulation of CXCR4 with gp120, can cause upregulation of TRAIL receptors and consequent sensitivity to apoptosis by this pathway. In this work, our aim was to measure if CD4+T lymphocytes from HIV+ patients, had and increased expression of TRAIL ligand and death receptors (DR) 5/4 and coreceptor CXCR4 and, evaluate its association Methods: Ten HIV+ ART naïve patients and seven HIV- donors were recruited. The immunophenotyping of CD4+T lymphocytes was performed with CD3+/CD4+ labeling, after that the TRAIL death receptors DR4 and DR5 as well as the TRAIL ligand and the coreceptor CXCR4 were measured for expression and MFI (median fluorescence intensity) by flow cytometry in whole blood samples Results: CD4+T lymphocytes from HIV+ patients showed an augmented expression and MFI of both death receptors and TRAIL ligand compared with the healthy controls; on the other hand, expression of coreceptor CXCR4 was increased in the HIV+ group and the MFI showed a significant difference compared to healthy subjects. Correlations between DR4 and the TRAIL ligand with CXCR4 showed no significance; in contrast, both expression and MFI of DR5 and CXCR5 were significant and showed a strong direct correlation (expression: p<0.05 r=0.69 and MFI: p<0.005 r=0.81). Conclusion: There is evidence of apoptosis triggered by CXCR4 activation, not related to the Fas pathway, which is one of the main causes related to cell depletion in HIV infection. The upregulation of the TRAIL pathway in HIV infected subjects is correlated with the CXCR4 expression, which could be the cause of the reported apoptosis in these patients. Disclosure: No significant relationships.