Sullivan D A, Yee L, Conner A S, Hann L E, Olivier M, Allansmith M R
Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts.
Immunology. 1990 Dec;71(4):573-80.
The objective of the present study was to determine whether antigenic presence on the ocular surface might directly influence the development or expression of the lacrimal secretory immune system. Experiments were designed to: (i) analyse the temporal accumulation of IgA-, IgG- and IgM-containing cells in lacrimal tissue during postnatal development (6-27 days of age); (ii) examine whether prevention of antigenic exposure to the ocular surface by unilateral tarsorrhaphy might inhibit lymphocyte immigration into the ipsilateral gland during development; and (iii) assess whether a non-invasive antigen, after placement on the ocular surface of infant or adult rats, undergoes retrograde transfer to the lacrimal gland. Our results demonstrated that: (i) the accumulation of IgA-, IgG- and IgM-containing cells in lacrimal tissue was most pronounced during the 6-day period after eyelid opening (15 days of age). The pattern of appearance of these Ig-containing cells, which were predominantly IgA-positive, was identical in both left and right lacrimal glands. (ii) Closure of the left lid by tarsorrhaphy from 10 to 18 days of age had no effect on the accumulation of IgA-, IgG- and IgM-containing cells in the left lacrimal tissue compared to cell numbers in the right gland. (iii) Following placement of radiolabelled albumin on the ocular surface, antigen was almost completely cleared within 1-2 hr. Analysis of lacrimal glands showed no significant accumulation of radioactivity at any time-point, either in the presence or absence of ocular inflammation. In contrast, up to 17.8% of radioactivity was found in the stomach 1-2 hr following topical antigen application. Overall, our results show that a rapid development of the lacrimal secretory immune system occurs between 15 and 21 days of age. This process does not appear to be dependent upon local antigenic stimulation. In addition, our findings indicate that a non-invasive antigen, when applied to the ocular surface, does not undergo retrograde transfer to the lacrimal gland. Instead, antigen appears to be cleared primarily through the gastrointestinal tract.
本研究的目的是确定眼表抗原的存在是否可能直接影响泪腺分泌免疫系统的发育或表达。实验设计如下:(i) 分析出生后发育阶段(6至27日龄)泪腺组织中含IgA、IgG和IgM细胞的时间积累情况;(ii) 研究通过单侧睑裂缝合防止眼表抗原暴露是否会抑制发育过程中淋巴细胞向同侧泪腺的迁移;(iii) 评估在将非侵入性抗原置于幼鼠或成年大鼠眼表后,抗原是否会逆行转移至泪腺。我们的结果表明:(i) 泪腺组织中含IgA、IgG和IgM细胞的积累在睁眼后6天(15日龄)最为明显。这些主要为IgA阳性的含Ig细胞的出现模式在左右泪腺中相同。(ii) 10至18日龄时通过睑裂缝合闭合左眼,与右侧泪腺中的细胞数量相比,对左侧泪腺组织中含IgA、IgG和IgM细胞的积累没有影响。(iii) 将放射性标记的白蛋白置于眼表后,抗原在1至2小时内几乎完全清除。泪腺分析显示,无论是否存在眼部炎症,在任何时间点均未发现放射性有明显积累。相比之下,局部应用抗原后1至2小时,胃中发现高达17.8%的放射性。总体而言,我们的结果表明,泪腺分泌免疫系统在15至21日龄之间迅速发育。这一过程似乎不依赖于局部抗原刺激。此外,我们的研究结果表明,非侵入性抗原应用于眼表后不会逆行转移至泪腺。相反,抗原似乎主要通过胃肠道清除。