Weintraub B C, Hedrick S M
Department of Biology, University of California, San Diego, USA.
Immunol Res. 1995;14(3):163-75. doi: 10.1007/BF02918214.
In most scientific investigations, the study of mechanism follows the study of function. For example, alpha beta T cells were shown to be important mediators of immunity before the interaction between the T cell receptor (TCR) and peptide-MHC complexes was understood. However, sometimes the study of function follows from the study of mechanism. Research of gamma delta T cell receptors falls into this category. The gamma chain of the TCR was first cloned in 1984, which then led to the discovery of gamma delta T cells in 1985. Since then, research has focused on understanding ligands of the gamma delta TCR with the hope of better understanding the function of gamma delta T cells. An initial assumption was that gamma delta T cells, like alpha beta T cells, recognize peptides bound to MHC molecules; however, recent data indicate that gamma delta T cells are not biased towards MHC recognition in the same way as alpha beta T cells. Although there are intriguing new insights, the specificity and function of gamma delta T cells remains a mystery.
在大多数科学研究中,对机制的研究是在对功能的研究之后进行的。例如,在人们了解T细胞受体(TCR)与肽 - MHC复合物之间的相互作用之前,αβ T细胞就已被证明是免疫的重要介质。然而,有时对功能的研究是基于对机制的研究。γδ T细胞受体的研究就属于这一类。TCR的γ链于1984年首次被克隆,随后在1985年发现了γδ T细胞。从那时起,研究重点一直是了解γδ TCR的配体,以期更好地理解γδ T细胞的功能。最初的假设是,γδ T细胞与αβ T细胞一样,识别与MHC分子结合的肽;然而,最近的数据表明,γδ T细胞不像αβ T细胞那样倾向于识别MHC。尽管有一些引人入胜的新见解,但γδ T细胞的特异性和功能仍然是个谜。