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Isolation of a monoclonal antibody from a phage display library binding the rhesus macaque MHC class I allomorph Mamu-A1*001

机译:从结合恒河猴MHC I类同种异型物Mamu-A1 * 001的噬菌体展示文库中分离单克隆抗体

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摘要

Monoclonal antibodies that bind to human leukocyte antigen (HLA) are useful tools for HLA-typing, tracking donor-recipient chimerisms after bone marrow transplants, and characterizing specific major histocompatibility complexes (MHC) on cell surfaces. Unfortunately, equivalent reagents are not available for rhesus macaques, which are commonly used animal as models in organ transplant and infectious disease research. To address this deficiency, we isolated an antibody that recognizes the common Indian rhesus macaque MHC class I molecule, Mamu-A1*001. We induced Mamu-A1*001-binding antibodies by alloimmunizing a female Mamu-A1*001-negative rhesus macaque with peripheral blood mononuclear cells (PBMC) from a male Mamu-A1*001-positive donor. A Fab phage display library was constructed with PBMC from the alloimmunized macaque and panned to isolate an antibody that binds to Mamu-A1*001 but not to other common rhesus macaque MHC class I molecules. The isolated antibody distinguishes PBMC from Mamu-A1*001-positive and -negative macaques. Additionally, the Mamu-A1*001-specific antibody binds the cynomolgus macaque MHC class I ortholog Mafa-A1*001:01 but not variants Mafa-A1*001:02/03, indicating a high degree of binding specificity. The Mamu-A1*001-specific antibody will be useful for identifying Mamu-A1*001-positive rhesus macaques, for detecting Mamu-A1*001-positive cells in populations of Mamu-A1*001-negative cells, and for examining disease processes that alter expression of Mamu-A1*001 on cell surfaces. Moreover, the alloimmunization process we describe will be useful for isolating additional MHC allomorph-specific monoclonal antibodies or antibodies against other polymorphic host proteins which are difficult to isolate with traditional technologies.
机译:结合人类白细胞抗原(HLA)的单克隆抗体是用于HLA分型,追踪骨髓移植后供体-受体嵌合体并表征细胞表面特定主要组织相容性复合物(MHC)的有用工具。不幸的是,恒河猴无法获得等效的试剂,恒河猴通常在器官移植和传染病研究中作为动物模型使用。为了解决这一缺陷,我们分离了一种识别常见印度猕猴MHC I类分子Mamu-A1 * 001的抗体。我们通过使用雄性Mamu-A1 * 001阳性供体的外周血单核细胞(PBMC)对雌性Mamu-A1 * 001阴性的恒河猴进行同种免疫,从而诱导了Mamu-A1 * 001的结合抗体。用来自同种免疫的猕猴的PBMC构建Fab噬菌体展示文库,淘选以分离与Mamu-A1 * 001结合但不与其他普通猕猴MHC I类分子结合的抗体。分离的抗体将PBMC与Mamu-A1 * 001阳性和阴性猕猴区分开。另外,Mamu-A1 * 001特异性抗体结合食蟹猕猴MHC I类直系同源物Mafa-A1 * 001:01,但不结合变体Mafa-A1 * 001:02/03,表明高度结合特异性。 Mamu-A1 * 001特异性抗体可用于鉴定Mamu-A1 * 001阳性恒河猴,检测Mamu-A1 * 001阴性细胞群中的Mamu-A1 * 001阳性细胞以及检查疾病改变Mamu-A1 * 001在细胞表面表达的过程。此外,我们描述的同种免疫过程将可用于分离其他MHC同种异体特异性单克隆抗体或针对传统技术难以分离的其他多态宿主蛋白的抗体。

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