首页> 美国卫生研究院文献>Immunology >Distribution of immunogenic cells after painting with the contact sensitizers fluorescein isothiocyanate and oxazolone. Different sensitizers form immunogenic complexes with different cell populations.
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Distribution of immunogenic cells after painting with the contact sensitizers fluorescein isothiocyanate and oxazolone. Different sensitizers form immunogenic complexes with different cell populations.

机译:涂有接触敏化剂异硫氰酸荧光素和恶唑酮的免疫原性细胞分布。不同的敏化剂形成具有不同细胞群的免疫原性复合物。

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摘要

The distribution of fluorescent cells in the draining lymph nodes of mice painted with the contact sensitizing agent fluorescein isothiocyanate (FITC) was investigated using a fluorescence-activated cell sorter. Up to 30% of the cells were fluorescent after 18 h and this decreased thereafter becoming undetectable after 4-5 days. Most of the fluorescent cells were morphologically lymphocytes, theta - ve and adherent to nylon wool. Immunogenicity of these cells was tested by injecting them into the footpads of normal mice and measuring contact sensitivity after 6 days. This was restricted to large cells which represented less than 5% of the white cell population and nearly all of which became fluorescent after skin painting. The large fluorescent cells were a mixture of monocytes and lymphocytes. Most of the lymphocytes had surface immunoglobulin. The immunogenicity was reduced by nylon filtration but was not affected by silica and anti-theta. These results showed that the immunogenicity is not associated with T cells. In contrast, similar immunogenic activity in the draining lymph nodes of mice painted with oxazolone is associated with T cells. The results therefore showed that different sensitizers form immunogenic complexes with different cell populations, perhaps in this case becuase of the different water solubilities of FITC and oxazolone. They also suggested that this may cause important differences in antigen presentation, for example in their association with different MHC products.
机译:使用荧光激活细胞分选仪研究了用接触敏化剂异硫氰酸荧光素(FITC)涂漆的小鼠的引流淋巴结中的荧光细胞分布。 18小时后,多达30%的细胞发荧光,此后下降,在4-5天后变得不可检测。从形态上讲,大多数荧光细胞是淋巴细胞,热流和粘附在尼龙绒上。通过将这些细胞注射到正常小鼠的脚垫中并在6天后测量接触敏感性来测试这些细胞的免疫原性。这仅限于代表白细胞总数不到5%的大细胞,并且几乎所有这些细胞在涂漆后都会变成荧光。大的荧光细胞是单核细胞和淋巴细胞的混合物。大多数淋巴细胞具有表面免疫球蛋白。尼龙过滤降低了免疫原性,但不受二氧化硅和抗θ的影响。这些结果表明免疫原性与T细胞无关。相反,用恶唑酮粉染的小鼠的引流淋巴结中类似的免疫原性活性与T细胞相关。因此,结果表明,不同的敏化剂与不同细胞群体形成免疫原性复合物,在这种情况下,可能是由于FITC和恶唑酮的水溶性不同。他们还建议,这可能会导致抗原呈递的重要差异,例如它们与不同的MHC产品的关联。

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