Kimura S, Kiyono H, Beagley K W, Torii M, Eldridge J H, Hamada S, Michalek S M, Koopman W J, McGhee J R
J Immunol. 1987 Jun 15;138(12):4387-94.
Our studies reported here, fully characterize two unique type 2 antigens trinitrophenol (TNP)-M1 serotype carbohydrates (TNP-M1 g and TNP-M1 c) derived from streptococci, which fail to induce antibody responses in xid or neonatal mouse splenic cultures. These antigens generate brisk responses in normal spleen and Peyer's patch cell cultures of xid mice, all of which suggest that responses are elicited in the Lyb-3+, 5+ B subpopulation. The antibody responses to TNP-M1 g (and TNP-M1 c) are not dependent upon T cells. Furthermore, TNP-M1 carbohydrates induce anti-TNP plaque-forming (PFC) responses in cultures of small, resting splenic B cell populations without an added T cell requirement. Thus two categories of type 2 antigens are distinguished, one which requires T cells or derived factors, e.g., TNP-Ficoll, and a second TNP-carbohydrate antigen TNP-M1 that does not. Studies of the mitogenic and polyclonal B cell activation properties of M1 carbohydrates indicated that B cell proliferation is induced in both xid (Lyb-3-, 5-) and normal (Lyb-3-, 5- and Lyb-3+, 5+) splenic B cell subpopulations, but that differentiation to IgM synthesis fails to occur in the Lyb-3-, 5- B cell subpopulation. Thus M1 carbohydrates are unique probes that allow the selective induction of proliferation and differentiation of mature B cells that are presumably Lyb-3+, 5+. Because the M1 serotype carbohydrates induce polyclonal IgM synthesis and antigen-specific responses in only the mature B cell population in the absence of T cells, whereas TNP-Ficoll and other type 2 antigens require T cells or their derived factors, the Lyb-3+, 5+ B cell subpopulation may consist of a T cell-dependent and a T cell-independent compartment for responses to different carbohydrate type 2 antigens.
我们在此报告的研究,全面表征了两种独特的2型抗原,即源自链球菌的三硝基苯酚(TNP)-M1血清型碳水化合物(TNP-M1 g和TNP-M1 c),它们在xid或新生小鼠脾脏培养物中无法诱导抗体反应。这些抗原在xid小鼠的正常脾脏和派伊尔结细胞培养物中引发强烈反应,所有这些都表明反应是在Lyb-3 +、5 + B亚群中引发的。对TNP-M1 g(和TNP-M1 c)的抗体反应不依赖于T细胞。此外,TNP-M1碳水化合物在未添加T细胞需求的小的、静止的脾脏B细胞群体培养物中诱导抗TNP空斑形成(PFC)反应。因此,区分出两类2型抗原,一类需要T细胞或其衍生因子,例如TNP-菲可,另一类是不需要的TNP-碳水化合物抗原TNP-M1。对M1碳水化合物的促有丝分裂和多克隆B细胞激活特性的研究表明,B细胞增殖在xid(Lyb-3 -、5 -)和正常(Lyb-3 -、5 -和Lyb-3 +、5 +)脾脏B细胞亚群中均被诱导,但在Lyb-3 -、5 - B细胞亚群中未能发生向IgM合成的分化。因此,M1碳水化合物是独特的探针,可选择性诱导可能是Lyb-3 +、5 +的成熟B细胞的增殖和分化。因为M1血清型碳水化合物仅在无T细胞的情况下在成熟B细胞群体中诱导多克隆IgM合成和抗原特异性反应,而TNP-菲可和其他2型抗原需要T细胞或其衍生因子,所以Lyb-3 +、5 + B细胞亚群可能由对不同2型碳水化合物抗原反应的T细胞依赖性和T细胞非依赖性区室组成。