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Deciphering the True Immunologic Risk in Renal Transplantation in Patients With HIV.
Kahler, Dylan; Curtis, Houston; Zhao, Huaqing; Diamond, Adam; Di Carlo, Antonio; Karhadkar, Sunil.
Affiliation
  • Kahler D; Department of Surgery, Temple University Hospital, Philadelphia, PA.
  • Curtis H; Lewis Katz School of Medicine at Temple University, Philadelphia, PA.
  • Zhao H; Center for Biostatistics and Epidemiology, Department of Biomedical Education and Data Science, Lewis Katz School of Medicine at Temple University, Philadelphia, PA.
  • Diamond A; Department of Pharmacy, Temple University Hospital, Philadelphia, PA.
  • Di Carlo A; Division of Abdominal Organ Transplant Surgery, Department of Surgery, Temple University Hospital, Philadelphia, PA.
  • Karhadkar S; Division of Abdominal Organ Transplant Surgery, Department of Surgery, Temple University Hospital, Philadelphia, PA. Electronic address: Sunil.Karhadkar@tuhs.temple.edu.
Transplant Proc ; 55(10): 2392-2397, 2023 Dec.
Article de En | MEDLINE | ID: mdl-37932184
ABSTRACT
Since 1995, rates of end-stage renal disease have risen dramatically in patients living with HIV infection. However, given the concern for higher rates of acute rejection in this patient population, the immunologic threat posed by HIV infection is a specter clinicians must continually confront. Living donor transplantation may negate this risk; this study aims to assess the benefit of living donor transplantation in this population and to ascertain the immunologic risk faced by patients who are HIV-infected. The 2021 UNOS database was queried, and all HIV-infected kidney transplant recipients since 1987 were identified. Recipients were stratified based on deceased (DDKT) vs living (LDKT) donor status. Overall survival, allograft survival, acute rejection, panel reactive antibody (PRA) percentage, and crossmatch positivity were compared between groups. One thousand two hundred twenty-six patients underwent DDKT, and 304 patients underwent LDKT. Living donor kidney transplantation demonstrated greater overall survival (P = .045) and graft survival (P < .001). However, no difference in acute rejection was noted between the cohorts, and no difference in overall or graft survival was evident based on PRA percentage. Crossmatch positive status did not negatively affect graft survival. Patients with HIV undergoing LDKT fared better than those undergoing DDKT. Nevertheless, patients at higher immunologic risk-elevated PRA% and crossmatch positivity-did not experience graft loss at a higher rate than patients at lower immunologic risk. These results were valid in both DDKT and LDKT cohorts. These findings suggest that infection with HIV does not overtly increase patients' immunologic risk, and concerns surrounding transplantation in this population may be overestimated.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Infections à VIH / Transplantation rénale Limites: Humans Langue: En Journal: Transplant Proc Année: 2023 Type de document: Article Pays d'affiliation: Panama

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Infections à VIH / Transplantation rénale Limites: Humans Langue: En Journal: Transplant Proc Année: 2023 Type de document: Article Pays d'affiliation: Panama