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DOI 10.1172/jci.insight.175375

Медицинская библиотека · JCI insight · 2024

Phase 1 trial evaluating safety and pharmacokinetics of HIV-1 broadly neutralizing mAbs 10E8VLS and VRC07-523LS.

Awan Seemal F, Pegu Amarendra, Strom Larisa, Carter Cristina A, Hendel Cynthia S, Holman LaSonji A, Costner Pamela J, Trofymenko Olga, Dyer Renunda, Gordon Ingelise J, Rothwell Ro Shauna S, Hickman Somia P, Conan-Cibotti Michelle, Doria-Rose Nicole A, Lin Bob C, O'Connell Sarah, Narpala Sandeep R, Almasri Cassandra G, Liu Cuiping, Ko Sungyoul, Kwon Young D, Namboodiri Aryan M, Pandey Janardan P, Arnold Frank J, Carlton Kevin, Gall Jason G, Kwong Peter D, Capparelli Edmund V, Bailer Robert T, McDermott Adrian B, Chen Grace L, Koup Richard A, Mascola John R, Coates Emily E, Ledgerwood Julie E, Gaudinski Martin R, VRC 610 study team

Клиническое исследование I фазыСтатьяResearch Support, N.I.H., IntramuralПеревод в очереди

Аннотация

BACKGROUNDBroadly neutralizing monoclonal antibodies (bNAbs) represent a promising strategy for HIV-1 immunoprophylaxis and treatment. 10E8VLS and VRC07-523LS are bNAbs that target the highly conserved membrane-proximal external region (MPER) and the CD4-binding site of the HIV-1 viral envelope glycoprotein, respectively.METHODSIn this phase 1, open-label trial, we evaluated the safety and pharmacokinetics of 5 mg/kg 10E8VLS administered alone, or concurrently with 5 mg/kg VRC07-523LS, via s.c. injection to healthy non-HIV-infected individuals.RESULTSEight participants received either 10E8VLS alone (n = 6) or 10E8VLS and VRC07-523LS in combination (n = 2). Five (n = 5 of 8, 62.5%) participants who received 10E8VLS experienced moderate local reactogenicity, and 1 participant (n = 1/8, 12.5%) experienced severe local reactogenicity. Further trial enrollment was stopped, and no participant received repeat dosing. All local reactogenicity resolved without sequelae. 10E8VLS retained its neutralizing capacity, and no functional anti-drug antibodies were detected; however, a serum t1/2 of 8.1 days was shorter than expected. Therefore, the trial was voluntarily stopped per sponsor decision (Vaccine Research Center, National Institute of Allergy and Infectious Diseases [NIAID], NIH). Mechanistic studies performed to investigate the underlying reason for the reactogenicity suggest that multiple mechanisms may have contributed, including antibody aggregation and upregulation of local inflammatory markers.CONCLUSION10E8VLS resulted in unexpected reactogenicity and a shorter t1/2 in comparison with previously tested bNAbs. These studies may facilitate identification of nonreactogenic second-generation MPER-targeting bNAbs, which could be an effective strategy for HIV-1 immunoprophylaxis and treatment.TRIAL REGISTRATIONClinicaltrials.gov, accession no. NCT03565315.FUNDINGDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH.

Для цитирования: Awan Seemal F, Pegu Amarendra, Strom Larisa, Carter Cristina A, Hendel Cynthia S, Holman LaSonji A, Costner Pamela J, Trofymenko Olga, Dyer Renunda, Gordon Ingelise J, Rothwell Ro Shauna S, Hickman Somia P, Conan-Cibotti Michelle, Doria-Rose Nicole A, Lin Bob C, O'Connell Sarah, Narpala Sandeep R, Almasri Cassandra G, Liu Cuiping, Ko Sungyoul, Kwon Young D, Namboodiri Aryan M, Pandey Janardan P, Arnold Frank J, Carlton Kevin, Gall Jason G, Kwong Peter D, Capparelli Edmund V, Bailer Robert T, McDermott Adrian B, Chen Grace L, Koup Richard A, Mascola John R, Coates Emily E, Ledgerwood Julie E, Gaudinski Martin R, VRC 610 study team. Phase 1 trial evaluating safety and pharmacokinetics of HIV-1 broadly neutralizing mAbs 10E8VLS and VRC07-523LS.. JCI insight. 2024. DOI: 10.1172/jci.insight.175375.

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