Tanimoto T, Ohtsuki Y
Chuo Meat Inspection Center, Kochi Prefectural Government, Tanimoto, Japan.
Am J Vet Res. 1996 Jun;57(6):853-9.
To determine whether antibodies raised against human or porcine lymphocytes are reactive with porcine lymphocytes and lymphoma cells in formalin-fixed, paraffin-embedded, antigen-retrieved tissue sections, and to determine the conditions suitable for antigen retrieval.
We evaluated reactivities of 27 anti-lymphocyte antibodies with porcine tissue sections, including those of lymphomas, treated with 11 antigen-retrieval methods.
Swine.
We used 19 anti-human and 8 anti-porcine lymphocyte antibodies. For antigen retrieval, we tested 11 methods: heating with 6 soaking solutions in a microwave oven, heating with 2 commercially available soaking solutions in a water bath, and enzyme digestion with 3 proteases. After these treatments, sections were immunostained along with untreated sections.
Of 27 anti-lymphocyte antibodies tested, CDw75 (clone LN-1), CD79 alpha (mb-1, clone HM57),CD79 beta (B29, clone B29/123), HLA-DR (clone TAL 1B5), and polyclonal CD3 were strongly reactive with porcine lymphoid tissues, including lymphomas, when sections were deparaffinized and heated in 0.1M Tris-HCl buffer (pH 8.0) in a microwave oven or with antigen-retrieval solution in a water bath. All patterns of positive staining were essentially the same as those previously described in human beings.
These 5 antibodies, with the antigen retrieval sequences, are helpful in identifying, distinguishing, and characterizing lymphocyte subsets in archival sections of normal and pathologic porcine lymphoid tissues including lymphomas. In addition, our findings indicated that antigen retrieval by microwave heating of the sections can appreciably expand the range of antibodies useful in paraffin immunohistochemistry, including those that otherwise work only on sections from frozen tissues or from an antigen-derived species.
确定针对人或猪淋巴细胞产生的抗体是否能与福尔马林固定、石蜡包埋、抗原修复组织切片中的猪淋巴细胞和淋巴瘤细胞发生反应,并确定适合抗原修复的条件。
我们评估了27种抗淋巴细胞抗体与猪组织切片(包括淋巴瘤组织切片)的反应性,这些组织切片采用了11种抗原修复方法进行处理。
猪。
我们使用了19种抗人淋巴细胞抗体和8种抗猪淋巴细胞抗体。对于抗原修复,我们测试了11种方法:在微波炉中用6种浸泡溶液加热、在水浴中用2种市售浸泡溶液加热以及用3种蛋白酶进行酶消化。经过这些处理后,切片与未处理的切片一起进行免疫染色。
在测试的27种抗淋巴细胞抗体中,当切片脱蜡并在微波炉中于0.1M Tris-HCl缓冲液(pH 8.0)中加热或在水浴中用抗原修复溶液处理时,CDw75(克隆LN-1)、CD79α(mb-1,克隆HM57)、CD79β(B29,克隆B29/123)、HLA-DR(克隆TAL 1B5)和多克隆CD3与包括淋巴瘤在内的猪淋巴组织有强烈反应。所有阳性染色模式与先前在人类中描述的基本相同。
这5种抗体以及抗原修复程序有助于识别、区分和鉴定正常和病理猪淋巴组织(包括淋巴瘤)存档切片中的淋巴细胞亚群。此外,我们的研究结果表明,通过对切片进行微波加热来进行抗原修复可以显著扩大石蜡免疫组织化学中可用抗体的范围,包括那些原本仅对冷冻组织切片或来自抗原源物种的切片起作用的抗体。