Jarvi Nicole L, Patel Manali, Shetty Krithika A, Nguyen Nhan H, Grasperge Brooke F, Mager Donald E, Straubinger Robert M, Balu-Iyer Sathy V
Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, United States.
Truvai Biosciences, LLC, Buffalo, NY, United States.
Front Immunol. 2024 Dec 10;15:1496169. doi: 10.3389/fimmu.2024.1496169. eCollection 2024.
Immunogenicity continues to be a challenge for development and clinical utility of monoclonal antibodies, and there are gaps in our current ability to prevent anti-drug antibody development in a safe and antigen-specific manner.
To mitigate immunogenicity of monoclonal antibodies administered subcutaneously, O-phospho-L-serine (OPLS)-the head group of the tolerance-inducing phospholipid, phosphatidylserine-was investigated as an immunoregulatory adjuvant.
Formulations of adalimumab, trastuzumab or rituximab with OPLS showed reduction in relative immunogenicity in mice compared to vehicle formulations, indicated by reduced anti-drug antibody development and significant reductions in CD138+ plasma cell differentiation in bone marrow. Titer development toward recombinant human hyaluronidase, a dispersion enhancer that was co-formulated with monoclonal antibodies, was similarly reduced. Subcutaneous administration of adalimumab with OPLS resulted in a two-fold increase in expression of type 1 regulatory (Tr1) T cell subset in the spleen. This is consistent with in vitro studies where co-culturing of dendritic cells primed with ovalbumin in the presence and absence of OPLS and antigen specific T-cells induced expression of Tr1 phenotype on live CD4+ T cells.
This adjuvant does not impact immune competence of non-human primates and mice, and repeated administration of the adjuvant does not show renal or hepatic toxicity. Formulation of monoclonal antibodies with the immunoregulatory adjuvant, OPLS, was found to be safe and effective at mitigating immunogenicity.
免疫原性仍然是单克隆抗体开发和临床应用面临的挑战,目前我们在以安全且抗原特异性的方式预防抗药物抗体产生方面的能力存在差距。
为减轻皮下注射单克隆抗体的免疫原性,研究了O-磷酸-L-丝氨酸(OPLS)——诱导耐受的磷脂磷脂酰丝氨酸的头部基团——作为一种免疫调节佐剂。
与赋形剂配方相比,阿达木单抗、曲妥珠单抗或利妥昔单抗与OPLS的配方在小鼠中显示出相对免疫原性降低,表现为抗药物抗体产生减少以及骨髓中CD138+浆细胞分化显著降低。针对与单克隆抗体共同配制的重组人透明质酸酶的滴度产生也同样降低。皮下注射阿达木单抗与OPLS导致脾脏中1型调节性(Tr1)T细胞亚群的表达增加了两倍。这与体外研究一致,即在存在和不存在OPLS的情况下用卵清蛋白致敏的树突状细胞与抗原特异性T细胞共同培养可诱导活CD4+ T细胞上Tr1表型的表达。
这种佐剂不会影响非人类灵长类动物和小鼠的免疫能力,并且重复给药该佐剂未显示出肾毒性或肝毒性。发现用免疫调节佐剂OPLS配制单克隆抗体在减轻免疫原性方面是安全有效的。