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Challenges and Opportunities of Therapies Targeting Early Life Immunity for Pediatric HIV Cure.
Berendam, Stella J; Nelson, Ashley N; Yagnik, Bhrugu; Goswami, Ria; Styles, Tiffany M; Neja, Margaret A; Phan, Caroline T; Dankwa, Sedem; Byrd, Alliyah U; Garrido, Carolina; Amara, Rama R; Chahroudi, Ann; Permar, Sallie R; Fouda, Genevieve G.
Affiliation
  • Berendam SJ; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
  • Nelson AN; Department of Pediatrics, Duke University School of Medicine, Durham, NC, United States.
  • Yagnik B; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
  • Goswami R; Department of Pediatrics, Duke University School of Medicine, Durham, NC, United States.
  • Styles TM; Department of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.
  • Neja MA; Department of Pediatrics, Weill Cornell Medicine, New York, NY, United States.
  • Phan CT; Department of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.
  • Dankwa S; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States.
  • Byrd AU; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
  • Garrido C; Department of Pediatrics, Weill Cornell Medicine, New York, NY, United States.
  • Amara RR; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
  • Chahroudi A; Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States.
  • Permar SR; Department of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA, United States.
  • Fouda GG; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States.
Front Immunol ; 13: 885272, 2022.
Article in En | MEDLINE | ID: mdl-35911681
ABSTRACT
Early initiation of antiretroviral therapy (ART) significantly improves clinical outcomes and reduces mortality of infants/children living with HIV. However, the ability of infected cells to establish latent viral reservoirs shortly after infection and to persist during long-term ART remains a major barrier to cure. In addition, while early ART treatment of infants living with HIV can limit the size of the virus reservoir, it can also blunt HIV-specific immune responses and does not mediate clearance of latently infected viral reservoirs. Thus, adjunctive immune-based therapies that are geared towards limiting the establishment of the virus reservoir and/or mediating the clearance of persistent reservoirs are of interest for their potential to achieve viral remission in the setting of pediatric HIV. Because of the differences between the early life and adult immune systems, these interventions may need to be tailored to the pediatric settings. Understanding the attributes and specificities of the early life immune milieu that are likely to impact the virus reservoir is important to guide the development of pediatric-specific immune-based interventions towards viral remission and cure. In this review, we compare the immune profiles of pediatric and adult HIV elite controllers, discuss the characteristics of cellular and anatomic HIV reservoirs in pediatric populations, and highlight the potential values of current cure strategies using immune-based therapies for long-term viral remission in the absence of ART in children living with HIV.
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Full text: 1 Database: MEDLINE Main subject: CD4-Positive T-Lymphocytes / HIV Infections Limits: Adult / Child / Humans / Infant Language: En Journal: Front Immunol Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: CD4-Positive T-Lymphocytes / HIV Infections Limits: Adult / Child / Humans / Infant Language: En Journal: Front Immunol Year: 2022 Type: Article Affiliation country: United States