CD1-restricted T cells: are unconventional allies the key to future TB vaccines?

被引:0
作者
Milton, Matthew [1 ]
Mansour, Salah [1 ,2 ]
机构
[1] Univ Southampton, Natl Inst Hlth Care Res NIHR, Fac Med, Biomed Res Ctr,Sch Clin & Expt Sci,, Southampton, England
[2] Univ Southampton, Inst Life Sci, Southampton, England
关键词
CD1; T cells; infection; tuberculosis; unconventional T cells; lipids; TB vaccine; BACILLUS-CALMETTE-GUERIN; CANDIDATE TUBERCULOSIS VACCINE; CD1 ANTIGEN PRESENTATION; MYCOBACTERIUM-TUBERCULOSIS; GAMMA-DELTA; CRYSTAL-STRUCTURE; LIPID ANTIGENS; IMMUNE-RESPONSES; FUNCTIONAL PLASTICITY; NONPEPTIDE ANTIGENS;
D O I
10.3389/fimmu.2025.1629466
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD1-restricted T cells constitute an unconventional arm of immunity that recognises lipid antigens, a feature particularly pertinent to Mycobacterium tuberculosis (Mtb), a pathogen with a lipid-rich cell wall. Unlike classical MHC-restricted responses, CD1-mediated lipid antigen presentation includes donor-unrestricted T cell responses, offering a promising pathway for universally protective tuberculosis (TB) vaccines. This review explores the biology of CD1 isoforms, the functional diversity of CD1-restricted T cell subsets, and their roles in TB immunity. We discuss Mtb's lipid antigens, mechanisms of CD1 trafficking and antigen presentation, immune evasion strategies, and emerging translational insights. By highlighting key knowledge gaps and future directions, we argue that harnessing CD1-restricted T cells could unlock novel vaccine strategies against the world's leading infectious killer.
引用
收藏
页数:16
相关论文
共 217 条
[31]   Activation of NKT cells protects mice from tuberculosis [J].
Chackerian, A ;
Alt, J ;
Perera, V ;
Behar, SM .
INFECTION AND IMMUNITY, 2002, 70 (11) :6302-6309
[32]   The versatility of the CD1 lipid antigen presentation pathway [J].
Chancellor, Andrew ;
Gadola, Stephan D. ;
Mansour, Salah .
IMMUNOLOGY, 2018, 154 (02) :196-203
[33]   Immune biology of Ag-specific γδ T cells in infections [J].
Chen, Zheng W. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (14) :2409-2417
[34]  
COLDITZ GA, 1995, PEDIATRICS, V96, P29
[35]   Human T cell epitopes of Mycobacterium tuberculosis are evolutionarily hyperconserved [J].
Comas, Inaki ;
Chakravartti, Jaidip ;
Small, Peter M. ;
Galagan, James ;
Niemann, Stefan ;
Kremer, Kristin ;
Ernst, Joel D. ;
Gagneux, Sebastien .
NATURE GENETICS, 2010, 42 (06) :498-U41
[36]   CD1a selectively captures endogenous cellular lipids that broadly block T cell response [J].
Cotton, Rachel N. ;
Wegrecki, Marcin ;
Cheng, Tan-Yun ;
Chen, Yi-Ling ;
Veerapen, Natacha ;
Le Nours, Jerome ;
Orgill, Dennis P. ;
Pomahac, Bohdan ;
Talbot, Simon G. ;
Willis, Richard ;
Altman, John D. ;
de Jong, Annemieke ;
Van Rhijn, Ildiko ;
Clark, Rachael A. ;
Besra, Gurdyal S. ;
Ogg, Graham ;
Rossjohn, Jamie ;
Moody, D. Branch .
JOURNAL OF EXPERIMENTAL MEDICINE, 2021, 218 (07)
[37]   Complex lipid determine tissue specific replication of Mycobacterium tuberculosis in mice [J].
Cox, JS ;
Chen, B ;
McNeil, M ;
Jacobs, WR .
NATURE, 1999, 402 (6757) :79-83
[38]   Casting a wider net: Immunosurveillance by nonclassical MHC molecules [J].
D'Souza, M. Patricia ;
Adams, Erin ;
Altman, John D. ;
Birnbaum, Michael E. ;
Boggiano, Cesar ;
Casorati, Giulia ;
Chien, Yueh-hsiu ;
Conley, Anthony ;
Eckle, Sidonia Barbara Guiomar ;
Fruh, Klaus ;
Gondre-Lewis, Timothy ;
Hassan, Namir ;
Huang, Huang ;
Jayashankar, Lakshmi ;
Kasmar, Anne G. ;
Kunwar, Nina ;
Lavelle, Judith ;
Lewinsohn, David M. ;
Moody, Branch ;
Picker, Louis ;
Ramachandra, Lakshmi ;
Shastri, Nilabh ;
Parham, Peter ;
McMichael, Andrew J. ;
Yewdell, Jonathan W. .
PLOS PATHOGENS, 2019, 15 (02)
[39]  
Dascher CC, 2007, CURR TOP MICROBIOL, V314, P3
[40]   Evolutionary constraints on CD1 structure: insights from comparative genomic analysis [J].
Dascher, CC ;
Brenner, MB .
TRENDS IN IMMUNOLOGY, 2003, 24 (08) :412-418