The immune response to HIV infection is poorly understood. Because of the tropism of the virus for cells of the immune system, it is not clear whether certain immunologic alterations reflect a protective host response to HIV or are indicative of immunopathology. Several lines of evidence suggest that there is protective immunity to HIV, particularly in HIV-exposed children. This evidence, along with the enormous social and ethical pressure to blunt the devastating epidemic of HIV in women and children, presents a rationale for ACTG-sponsored immune based therapies for amelioration and prevention of HIV disease. The in vitro testing of cellular and humoral immune function is essential for evaluation of the impact of experimental immune based therapies for HIV infection. The UCLA Pediatric ACTU has the capability to test host immune function through a consortium of immunology laboratories in the Center for the Health Sciences. The laboratories have the capability to: 1) Characterize the level of HIV-specific cellular immunity in response to vaccine or other immunomodulatory therapy utilizing assays of lymphocyte proliferation to HIV proteins and cytotoxicity of T cells to HIV-expressing target cells, 2) Assess HIV-specific humoral immunity in response to active or passive immunization utilizing assays for neutralizing antibody and antibody-dependent cellular cytotoxicity, 3) Assess general cellular immunity by non-HIV specific antigen responses utilizing assays of lymphocyte proliferation to mitogens and non-HIV microbial antigens, 4) Characterize decreased immune activation as a marker of therapeutic efficacy utilizing assays for flow cytometric determination of cell surface activation antigen expression, serum cytokine and soluble activation molecule levels, and cellular expression of mRNA for cytokines. The assays are performed according to available approved or recommended ACTG protocols. The expertise to perform these assays is available at UCLA along with the leadership evidenced by the participation of the Investigators in numerous Immunology and Pediatric Working Groups and Committees within the ACTG.

Project Start
Project End
Budget Start
Budget End
Support Year
9
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Sha, Beverly E; Tierney, Camlin; Cohn, Susan E et al. (2011) Postpartum viral load rebound in HIV-1-infected women treated with highly active antiretroviral therapy: AIDS Clinical Trials Group Protocol A5150. HIV Clin Trials 12:9-23
Veloso, Valdiléa G; Bastos, Francisco I; Portela, Margareth Crisóstomo et al. (2010) HIV rapid testing as a key strategy for prevention of mother-to-child transmission in Brazil. Rev Saude Publica 44:803-11
Truong, Hong-Ha M; Sim, Myung S; Dillon, Maryanne et al. (2010) Correlation of immune activation during late pregnancy and early postpartum with increases in plasma HIV RNA, CD4/CD8 T cells, and serum activation markers. Clin Vaccine Immunol 17:2024-8
Aldrovandi, Grace M; Chu, Clara; Shearer, William T et al. (2009) Antiretroviral exposure and lymphocyte mtDNA content among uninfected infants of HIV-1-infected women. Pediatrics 124:e1189-97
Bryson, Y J; Mirochnick, M; Stek, A et al. (2008) Pharmacokinetics and safety of nelfinavir when used in combination with zidovudine and lamivudine in HIV-infected pregnant women: Pediatric AIDS Clinical Trials Group (PACTG) Protocol 353. HIV Clin Trials 9:115-25
Fletcher, Courtney V; DeVille, Jaime G; Samson, Pearl M et al. (2007) Nonlinear pharmacokinetics of high-dose recombinant fusion protein CD4-IgG2 (PRO 542) observed in HIV-1-infected children. J Allergy Clin Immunol 119:747-50
Ching, Natascha; Yang, Otto O; Deville, Jaime G et al. (2007) Pediatric HIV-1-specific cytotoxic T-lymphocyte responses suggesting ongoing viral replication despite combination antiretroviral therapy. Pediatr Res 61:692-7
Shearer, William T; DeVille, Jaime G; Samson, Pearl M et al. (2006) Susceptibility of pediatric HIV-1 isolates to recombinant CD4-IgG2 (PRO 542) and humanized mAb to the chemokine receptor CCR5 (PRO 140). J Allergy Clin Immunol 118:518-21
Lambert, John S; Moye Jr, Jack; Plaeger, Susan F et al. (2005) Association of selected phenotypic markers of lymphocyte activation and differentiation with perinatal human immunodeficiency virus transmission and infant infection. Clin Diagn Lab Immunol 12:622-31
Watts, D Heather; Lambert, John; Stiehm, E Richard et al. (2003) Progression of HIV disease among women following delivery. J Acquir Immune Defic Syndr 33:585-93

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