Dunkley M L, Husband A J
Faculty of Medicine, University of Newcastle, New South Wales, Australia.
Immunology. 1987 Aug;61(4):475-82.
Antigen-specific T-helper cells for IgA responses arise in Peyer's patches (PP) following their immunization by subserosal injection of keyhole limpet haemocyanin (KLH). These are of the W3/25 phenotype and the W3/25 receptor is shown here to be involved in their helper function. These cells originate in PP and migrate via mesenteric lymph nodes (MLN) to thoracic duct lymph, although the MLN appear to be unnecessary for the induction or maturation of antigen-specific helper cells collected in thoracic duct lymph after intra-Peyer's patch (i.p.p.) immunization. KLH-specific helper cells can be detected subsequently in the intraepithelial lymphocyte population and also among lamina propria lymphocytes. The helper cells also relocate to PP distant to their site of origin where they are retained only when antigen is present. While i.p.p. immunization is an efficient route for the induction of IgA helper cells in gut-associated lymphoid tissue, it differs from oral immunization in that concomitant induction of antigen-specific splenic suppressor cells does not occur, indicating a role for epithelial antigen processing in this phenomenon.
通过浆膜下注射钥孔戚血蓝蛋白(KLH)免疫后,派尔集合淋巴结(PP)中会产生针对IgA应答的抗原特异性辅助性T细胞。这些细胞具有W3/25表型,并且本文显示W3/25受体参与其辅助功能。这些细胞起源于PP,经肠系膜淋巴结(MLN)迁移至胸导管淋巴,不过在派尔集合淋巴结内(i.p.p.)免疫后,胸导管淋巴中收集到的抗原特异性辅助细胞的诱导或成熟似乎并不需要MLN。随后可在上皮内淋巴细胞群体以及固有层淋巴细胞中检测到KLH特异性辅助细胞。这些辅助细胞还会迁移至远离其起源部位的PP,只有当存在抗原时它们才会在那里停留。虽然i.p.p.免疫是在肠道相关淋巴组织中诱导IgA辅助细胞的有效途径,但它与口服免疫不同,因为不会同时诱导抗原特异性脾抑制细胞,这表明上皮抗原加工在这一现象中起作用。