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CBA小鼠对经辐照与经甲醛固定的同种异体莫洛尼淋巴瘤细胞的同种特异性和病毒特异性免疫反应的比较。

Comparison of the allospecific and viral-specific immune responses to irradiated versus formaldehyde-fixed allogeneic Moloney lymphoma cells in CBA mice.

作者信息

Lamon E W, Gatti R A, Kiessling R, Fenyö E M

出版信息

Cancer Res. 1975 Apr;35(4):962-9.

PMID:1090367
Abstract

Two groups of adult CBA mice were immunized with 10-7 allogeneic Moloney lymphoma (YAC) cells. These YAC (H-2a) cells, which were either irradiated with 6000 R (Group i) or were formaldehyde fixed (Group II), were injected i.p. at weekly intervals for 3 weeks. Four days following the last injection, sera and lymphocytes were collected and tested in vitro for activity against either allospecific antigens (H-2d target cells) or viral-specific antigens, namely, Moloney leukemia virus (MLV). Both groups of animals developed measurable cellular and humoral immunity to the virally determined antigens. However, only the animals in Group i, immunized with irradiated cells, developed detectable immunity to H-2d. Immune and control lymphocytes were tested in microcytotoxicity tests and by 51Cr release. Antibody was assessed by complement-dependent cytotoxicity, indirect membrane immunofluorescence, virus neutralization, and antibody-dependent lymphocyte cytotoxicity. Group I serum, which had both anti-MLV and anti-H-2 antibodies, was absorbed with either living or formaldehyde-fixed YAC cells. The living cells were able to remove both H-2 and MLV antibodies. On the other hand, the formaldehyde-fixed cells removed no H-2 antibody but were able to remove MLV antibody, although less efficiently than living cells. These data indicate that formaldehyde fixation selectively impaired the H-2 antigens, leaving the viral antigenicity relatively intact. Differences between the immune responses to MLV-determined antigens and to H-2 antigens were demonstrated in many of the parallel in vitro tests.

摘要

将两组成年CBA小鼠用10⁻⁷个同种异体莫洛尼淋巴瘤(YAC)细胞进行免疫。这些YAC(H-2a)细胞,一组用6000伦琴进行照射(第一组),另一组用甲醛固定(第二组),每周腹腔注射一次,共注射3周。最后一次注射后4天,收集血清和淋巴细胞,并在体外检测其对同种特异性抗原(H-2d靶细胞)或病毒特异性抗原,即莫洛尼白血病病毒(MLV)的活性。两组动物均对病毒决定的抗原产生了可测量的细胞免疫和体液免疫。然而,只有用照射过的细胞免疫的第一组动物对H-2d产生了可检测到的免疫。免疫淋巴细胞和对照淋巴细胞通过微量细胞毒性试验和⁵¹Cr释放试验进行检测。抗体通过补体依赖的细胞毒性、间接膜免疫荧光、病毒中和以及抗体依赖的淋巴细胞细胞毒性进行评估。含有抗MLV和抗H-2抗体的第一组血清用活的或甲醛固定的YAC细胞进行吸收。活细胞能够去除H-2和MLV抗体。另一方面,甲醛固定的细胞不能去除H-2抗体,但能够去除MLV抗体,尽管效率低于活细胞。这些数据表明,甲醛固定选择性地损害了H-2抗原,而使病毒抗原性相对完整。在许多平行的体外试验中都证明了对MLV决定的抗原和对H-2抗原的免疫反应之间的差异。

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