MicroRNA-150 Is a Potential Biomarker of HIV/AIDS Disease Progression and Therapy
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作者:
Munshi, Saif Ullah
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Int Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, IndiaInt Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, India
Munshi, Saif Ullah
[1
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Panda, Harekrushna
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Int Ctr Genet Engn & Biotechnol, ICGEB Emory Vaccine Ctr, New Delhi, IndiaInt Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, India
Panda, Harekrushna
[2
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Holla, Prasida
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Int Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, IndiaInt Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, India
Holla, Prasida
[1
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Rewari, Bharat Bhushan
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Natl AIDS Control Org, ART Dept, New Delhi, India
Dr Ram Manohar Lohia Hosp, New Delhi, IndiaInt Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, India
Rewari, Bharat Bhushan
[3
,4
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Jameel, Shahid
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Int Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, IndiaInt Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, India
Jameel, Shahid
[1
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机构:
[1] Int Ctr Genet Engn & Biotechnol, Virol Grp, New Delhi, India
[2] Int Ctr Genet Engn & Biotechnol, ICGEB Emory Vaccine Ctr, New Delhi, India
[3] Natl AIDS Control Org, ART Dept, New Delhi, India
Background: The surrogate markers of HIV/AIDS progression include CD4 T cell count and plasma viral load. But, their reliability has been questioned in patients on anti-retroviral therapy (ART). Five microRNAs (miRNAs) - miR-16, miR-146b-5p, miR-150, miR-191 and miR-223 in peripheral blood mononuclear cells (PBMCs) were earlier found to assign HIV/AIDS patients into groups with varying CD4 T cell counts and viral loads. In this pilot study, we profiled the expression of these five miRNAs in PBMCs, and two of these miRNAs (miR-146b-5p and miR-150) in the plasma of HIV/AIDS patients, including those on ART and those who developed ART resistance, to evaluate if these are biomarkers of disease progression and therapy. Results: We quantified miRNA levels by quantitative reverse transcription polymerase chain reaction (qRT-PCR) using RNA isolated from PBMCs and plasma of healthy persons or HIV-infected patients who were (1) asymptomatic; (2) symptomatic and ART naive; (3) on ART; and (4) failing ART. Our results show miR-150 (p<0.01) and to a lesser extent miR-146b-5p (p<0.05) levels in PBMCs to reliably distinguish between ART-naive AIDS patients, those on ART, and those developing drug resistance and failing ART. The plasma levels of these two miRNAs also varied significantly between patients in these groups and between patients and healthy controls (p values <0.05). Conclusions: We report for the first time that PBMC and plasma levels of miR-150 and miR-146b-5p are predictive of HIV/AIDS disease progression and therapy.