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DOI 10.1172/jci.insight.160964

Медицинская библиотека · JCI insight · 2022

Randomized phase I trial of antigen-specific tolerizing immunotherapy with peptide/calcitriol liposomes in ACPA+ rheumatoid arthritis.

Sonigra Amee, Nel Hendrik J, Wehr Pascale, Ramnoruth Nishta, Patel Swati, van Schie Karin A, Bladen Maxwell W, Mehdi Ahmed M, Tesiram Joanne, Talekar Meghna, Rossjohn Jamie, Reid Hugh H, Stuurman Frederik E, Roberts Helen, Vecchio Phillip, Gourley Ian, Rigby Mark, Becart Stephane, Toes Rene Em, Scherer Hans Ulrich, Lê Cao Kim-Anh, Campbell Kim, Thomas Ranjeny

Клиническое исследование I фазыРандомизированное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUNDAntigen-specific regulation of autoimmune disease is a major goal. In seropositive rheumatoid arthritis (RA), T cell help to autoreactive B cells matures the citrullinated (Cit) antigen-specific immune response, generating RA-specific V domain glycosylated anti-Cit protein antibodies (ACPA VDG) before arthritis onset. Low or escalating antigen administration under "sub-immunogenic" conditions favors tolerance. We explored safety, pharmacokinetics, and immunological and clinical effects of s.c. DEN-181, comprising liposomes encapsulating self-peptide collagen II259-273 (CII) and NF-κB inhibitor 1,25-dihydroxycholecalciferol.METHODSA double-blind, placebo-controlled, exploratory, single-ascending-dose, phase I trial assessed the impact of low, medium, and high DEN-181 doses on peripheral blood CII-specific and bystander Cit64vimentin59-71-specific (Cit-Vim-specific) autoreactive T cell responses, cytokines, and ACPA in 17 HLA-DRB1*04:01+ or *01:01+ ACPA+ RA patients on methotrexate.RESULTSDEN-181 was well tolerated. Relative to placebo and normalized to baseline values, Cit-Vim-specific T cells decreased in patients administered medium and high doses of DEN-181. Relative to placebo, percentage of CII-specific programmed cell death 1+ T cells increased within 28 days of DEN-181. Exploratory analysis in DEN-181-treated patients suggested improved RA disease activity was associated with expansion of CII-specific and Cit-Vim-specific T cells; reduction in ACPA VDG, memory B cells, and inflammatory myeloid populations; and enrichment in CCR7+ and naive T cells. Single-cell sequencing identified T cell transcripts associated with tolerogenic TCR signaling and exhaustion after low or medium doses of DEN-181.CONCLUSIONThe safety and immunomodulatory activity of low/medium DEN-181 doses provide rationale to further assess antigen-specific immunomodulatory therapy in ACPA+ RA.TRIAL REGISTRATIONAnzctr.org.au identifier ACTRN12617001482358, updated September 8, 2022.FUNDINGInnovative Medicines Initiative 2 Joint Undertaking (grant agreement 777357), supported by European Union's Horizon 2020 research and innovation programme and European Federation of Pharmaceutical Industries and Associations; Arthritis Queensland; National Health and Medical Research Council (NHMRC) Senior Research Fellowship; and NHMRC grant 2008287.

Для цитирования: Sonigra Amee, Nel Hendrik J, Wehr Pascale, Ramnoruth Nishta, Patel Swati, van Schie Karin A, Bladen Maxwell W, Mehdi Ahmed M, Tesiram Joanne, Talekar Meghna, Rossjohn Jamie, Reid Hugh H, Stuurman Frederik E, Roberts Helen, Vecchio Phillip, Gourley Ian, Rigby Mark, Becart Stephane, Toes Rene Em, Scherer Hans Ulrich, Lê Cao Kim-Anh, Campbell Kim, Thomas Ranjeny. Randomized phase I trial of antigen-specific tolerizing immunotherapy with peptide/calcitriol liposomes in ACPA+ rheumatoid arthritis.. JCI insight. 2022. DOI: 10.1172/jci.insight.160964.

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