Efficient generation of monoclonal antibodies against peptide in the context of MHCII using magnetic enrichment

被引:27
作者
Spanier, Justin A. [1 ]
Frederick, Daniel R. [2 ]
Taylor, Justin J. [3 ,5 ]
Heffernan, James R. [1 ]
Kotov, Dmitri I. [3 ]
Martinov, Tijana [1 ]
Osum, Kevin C. [1 ]
Ruggiero, Jenna L. [1 ]
Rust, Blake J. [4 ]
Landry, Samuel J. [4 ]
Jenkins, Marc K. [3 ]
McLachlan, James B. [2 ]
Fife, Brian T. [1 ]
机构
[1] Univ Minnesota, Dept Med, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
[2] Tulane Univ, Dept Microbiol & Immunol, Sch Med, New Orleans, LA 70112 USA
[3] Univ Minnesota, Dept Microbiol & Immunol, Ctr Immunol, Sch Med, Minneapolis, MN 55455 USA
[4] Tulane Univ, Dept Biochem, Sch Med, New Orleans, LA 70112 USA
[5] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98019 USA
关键词
CD4(+) T-CELLS; SELF-PEPTIDE; NOD MICE; ANTIGEN; PD-1; IDENTIFICATION; SPECIFICITY; INFECTION; COMPLEX; AUTOIMMUNITY;
D O I
10.1038/ncomms11804
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Monoclonal antibodies specific for foreign antigens, auto-antigens, allogeneic antigens and tumour neo-antigens in the context of major histocompatibility complex II (MHCII) are highly desirable as novel immunotherapeutics. However, there is no standard protocol for the efficient generation of monoclonal antibodies that recognize peptide in the context of MHCII, and only a limited number of such reagents exist. In this report, we describe an approach for the generation and screening of monoclonal antibodies specific for peptide bound to MHCII. This approach exploits the use of recombinant peptide: MHC monomers as immunogens, and subsequently relies on multimers to pre-screen and magnetically enrich the responding antigen-specific B cells before fusion and validation, thus saving significant time and reagents. Using this method, we have generated two antibodies enabling us to interrogate antigen presentation and T-cell activation. This methodology sets the standard to generate monoclonal antibodies against the peptide-MHCII complexes.
引用
收藏
页数:11
相关论文
共 37 条
[1]   A T cell receptor-specific blockade of positive selection [J].
Baldwin, KK ;
Reay, PA ;
Wu, L ;
Farr, A ;
Davis, MM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (01) :13-23
[2]   Characterization and quantitation of peptide-MHC complexes produced from hen egg lysozyme using a monoclonal antibody [J].
Dadaglio, G ;
Nelson, CA ;
Deck, MB ;
Petzold, SJ ;
Unanue, ER .
IMMUNITY, 1997, 6 (06) :727-738
[3]   Ex vivo analysis of human memory CD4 T cells specific for hepatitis C virus using MHC class II tetramers [J].
Day, CL ;
Seth, NP ;
Lucas, M ;
Appel, H ;
Gauthier, L ;
Lauer, GM ;
Robbins, GK ;
Szczepiorkowski, ZM ;
Casson, DR ;
Chung, RT ;
Bell, S ;
Harcourt, G ;
Walker, BD ;
Klenerman, P ;
Wucherpfennig, KW .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (06) :831-842
[4]   Selective Priming and Expansion of Antigen-Specific Foxp3-CD4+ T Cells during Listeria monocytogenes Infection [J].
Ertelt, James M. ;
Rowe, Jared H. ;
Johanns, Tanner M. ;
Lai, Joseph C. ;
McLachlan, James B. ;
Way, Sing Sing .
JOURNAL OF IMMUNOLOGY, 2009, 182 (05) :3032-3038
[5]   Control of peripheral T-cell tolerance and autoimmunity via the CTLA-4 and PD-1 pathways [J].
Fife, Brian T. ;
Bluestone, Jeffrey A. .
IMMUNOLOGICAL REVIEWS, 2008, 224 :166-182
[6]   Insulin-induced remission in new-onset NOD mice is maintained by the PD-1-PD-L1 pathway [J].
Fife, Brian T. ;
Guleria, Indira ;
Bupp, Melanie Gubbels ;
Eagar, Todd N. ;
Tang, Qizhi ;
Bour-Jordan, Helene ;
Yagita, Hideo ;
Azuma, Miyuki ;
Sayegh, Mohamed H. ;
Bluestone, Jeffrey A. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (12) :2737-2747
[7]   Interactions between PD-1 and PD-L1 promote tolerance by blocking the TCR-induced stop signal [J].
Fife, Brian T. ;
Pauken, Kristen E. ;
Eagar, Todd N. ;
Obu, Takashi ;
Wu, Jenny ;
Tang, Qizhi ;
Azuma, Miyuki ;
Krummel, Matthew F. ;
Bluestone, Jeffrey A. .
NATURE IMMUNOLOGY, 2009, 10 (11) :1185-U70
[8]   LYMPHOCYTE-T CLONE SPECIFIC FOR PANCREATIC-ISLET ANTIGEN [J].
HASKINS, K ;
PORTAS, M ;
BRADLEY, B ;
WEGMANN, D ;
LAFFERTY, K .
DIABETES, 1988, 37 (10) :1444-1448
[9]  
JANEWAY CA, 1984, J IMMUNOL, V132, P662
[10]   Identification of MHC class II-restricted peptide ligands, including a glutamic acid decarboxylase 65 sequence, that stimulate diabetogenic T cells from transgenic BDC2.5 nonobese diabetic mice [J].
Judkowski, V ;
Pinilla, C ;
Schroder, K ;
Tucker, L ;
Sarvetnick, N ;
Wilson, DB .
JOURNAL OF IMMUNOLOGY, 2001, 166 (02) :908-917