PMID- 27212842 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20160523 LR - 20200930 IS - 0973-2063 (Print) IS - 0973-2063 (Electronic) IS - 0973-2063 (Linking) VI - 12 IP - 1 DP - 2016 TI - Hypothalamus-Pituitary-Adrenal cell-mediated immunity regulation in the Immune Restoration Inflammatory Syndrome. PG - 28-31 LID - 10.6026/97320630012028 [doi] AB - Over one third of the patients sero-positive for the human immunodeficiency virus (HIV) with signs of the acquired immune deficiency syndrome (AIDS), and under treatment with anti-retroviral therapy (ART), develop the immune reconstitution inflammatory syndrome (IRIS). It is not clear what variables are that determine whether a patient with HIV/AIDS will develop ART-related IRIS, but the best evidence base thus far indicates that HIV/AIDS patients with low CD4 cell count, and HIV/AIDS patients whose CD4 count recovery shows a sharp slope, suggesting a particularly fast "immune reconstitution", are at greater risk of developing IRIS. Here, we propose the hypothesis that one important variable that can contribute to low CD4 cell count number and function in ART-treated HIV/AIDS patients is altered hypothalamic-pituitary-adrenal (HPA) cell-mediated immune (CMI) regulation. We discuss HPA-CMI deregulation in IRIS as the new frontier in comparative effectiveness research (CRE) for obtaining and utilizing the best evidence base for treatment of patients with HIV/AIDS in specific clinical settings. We propose that our hypothesis about altered HPA-CMI may extend to the pathologies observed in related viral infection, including Zika. FAU - Khakshooy, Allen AU - Khakshooy A AD - Oral Biology and Medicine, Center for the health Sciences University of California Los Angeles, USA; Health Sciences, California State University, Northridge, USA. FAU - Chiappelli, Francesco AU - Chiappelli F AD - Oral Biology and Medicine, Center for the health Sciences University of California Los Angeles, USA; Evidence-Based Decisions Practice-Based Research Network, USA. LA - eng PT - Journal Article DEP - 20160131 PL - Singapore TA - Bioinformation JT - Bioinformation JID - 101258255 PMC - PMC4857463 EDAT- 2016/05/24 06:00 MHDA- 2016/05/24 06:01 PMCR- 2016/01/01 CRDT- 2016/05/24 06:00 PHST- 2016/01/31 00:00 [received] PHST- 2016/01/31 00:00 [accepted] PHST- 2016/05/24 06:00 [entrez] PHST- 2016/05/24 06:00 [pubmed] PHST- 2016/05/24 06:01 [medline] PHST- 2016/01/01 00:00 [pmc-release] AID - 97320630012028 [pii] AID - 10.6026/97320630012028 [doi] PST - epublish SO - Bioinformation. 2016 Jan 31;12(1):28-31. doi: 10.6026/97320630012028. eCollection 2016.