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1
The Qa2 subregion controls the expression of two antigens recognized by H-2-unrestricted cytotoxic T cells.Qa2亚区控制两种可被H-2非限制性细胞毒性T细胞识别的抗原的表达。
J Exp Med. 1982 Mar 1;155(3):749-67. doi: 10.1084/jem.155.3.749.
2
Qa-1-associated antigens. IV. Evidence for additional Qa-1 polymorphism defined biochemically and by cytotoxic T lymphocyte recognition.Qa-1相关抗原。IV. 通过生化方法及细胞毒性T淋巴细胞识别所定义的Qa-1额外多态性的证据。
Transplantation. 1982 Jul;34(1):54-9.
3
H-2 unrestricted cytotoxic T cell activity against antigens controlled by genes in the QA/TLA region.针对由QA/TLA区域基因控制的抗原的H-2非限制性细胞毒性T细胞活性。
J Immunol. 1979 Dec;123(6):2451-5.
4
Helper activity is required for the in vivo generation of cytotoxic T lymphocytes.体内细胞毒性T淋巴细胞的生成需要辅助活性。
J Exp Med. 1982 Mar 1;155(3):768-82. doi: 10.1084/jem.155.3.768.
5
The Qa-1 alloantigens. II. Evidence for the expression of two Qa-1 molecules by the Qa-1d genotype and for cross-reactivity between Qa-1 and H-2K.Qa-1同种异体抗原。II. Qa-1d基因型表达两种Qa-1分子以及Qa-1与H-2K之间存在交叉反应性的证据。
J Immunol. 1983 Mar;130(3):1293-9.
6
Biology of cloned cytotoxic T lymphocytes specific for lymphocytic choriomeningitis virus. I. Generation and recognition of virus strains and H-2b mutants.针对淋巴细胞性脉络丛脑膜炎病毒的克隆化细胞毒性T淋巴细胞的生物学特性。I. 病毒株及H-2b突变体的产生与识别
J Immunol. 1984 Jul;133(1):433-9.
7
Characterization of determinants encoded by four Qa-1 genotypes and their recognition by cloned cytotoxic T lymphocytes.四种Qa-1基因型所编码决定簇的特性及其被克隆的细胞毒性T淋巴细胞识别的情况。
J Immunol. 1983 Nov;131(5):2147-53.
8
H-2L-restricted recognition of viral antigens In the H-2d haplotype, anti-vesicular stomatitis virus cytotoxic T cells are restricted solely by H-2L.H-2L对病毒抗原的限制性识别 在H-2d单倍型中,抗水泡性口炎病毒细胞毒性T细胞仅受H-2L的限制。
J Exp Med. 1982 Sep 1;156(3):778-90. doi: 10.1084/jem.156.3.778.
9
Induction and characterization of minor histocompatibility antigens. Specific primary cytotoxic T lymphocyte responses in vitro.次要组织相容性抗原的诱导与特性。体外特异性原发性细胞毒性T淋巴细胞反应。
J Immunol. 1988 Feb 1;140(3):723-9.
10
The target minor H antigen for F1 cytotoxic T lymphocytes induced by Igh-congenic parental spleen cells is coded for by gene linked to H-2.由同基因亲本脾脏细胞诱导的F1细胞毒性T淋巴细胞的靶次要组织相容性抗原由与H-2相关的基因编码。
J Immunol. 1985 May;134(5):2953-9.

引用本文的文献

1
An MHC class Ib-restricted CD8 T cell response confers antiviral immunity.MHC Ib类限制性CD8 T细胞应答赋予抗病毒免疫力。
J Exp Med. 2008 Jul 7;205(7):1647-57. doi: 10.1084/jem.20080570. Epub 2008 Jun 9.
2
Availability of endogenous peptides limits expression of an M3a-Ld major histocompatibility complex class I chimera.内源性肽的可用性限制了M3a-Ld主要组织相容性复合体I类嵌合体的表达。
J Exp Med. 1994 Jan 1;179(1):155-65. doi: 10.1084/jem.179.1.155.
3
The alpha 3 domain of the Qa-2 molecule is defective for CD8 binding and cytotoxic T lymphocyte activation.Qa-2分子的α3结构域在与CD8结合及细胞毒性T淋巴细胞激活方面存在缺陷。
J Exp Med. 1993 Dec 1;178(6):2139-45. doi: 10.1084/jem.178.6.2139.
4
Syngeneic tumor immunizations produce Qa antibodies. Discovery of a new Qa antigen, Qa-6.同基因肿瘤免疫接种产生Qa抗体。一种新的Qa抗原Qa-6的发现。
Immunogenetics. 1982;16(4):329-37. doi: 10.1007/BF00372304.
5
Genetic analysis of the T-H-2 region in non-t chromosomes. I. Two new congenic strains isolate Qglo-1 from H-2.非T染色体上T-H-2区域的遗传分析。I. 从H-2分离出的两个新的同类系菌株Qglo-1。
Immunogenetics. 1983;17(5):445-55. doi: 10.1007/BF00696868.
6
Genetic control of minor histocompatibility antigens in the mouse.小鼠次要组织相容性抗原的遗传控制
Surv Immunol Res. 1984;3(2-3):184-6. doi: 10.1007/BF02918790.
7
The H-2dm1 mutation and Qa antigens.H-2dm1突变与Qa抗原。
Immunogenetics. 1983;18(6):617-24. doi: 10.1007/BF00345969.
8
Serologic cross-reactivity between Class I MHC molecules and an H-2-linked differentiation antigen as detected by monoclonal antibodies.通过单克隆抗体检测到的I类主要组织相容性复合体分子与H-2连锁分化抗原之间的血清学交叉反应性。
J Exp Med. 1984 Jan 1;159(1):21-40. doi: 10.1084/jem.159.1.21.
9
Expression in L cells of transfected class I genes from the mouse major histocompatibility complex.小鼠主要组织相容性复合体转染的I类基因在L细胞中的表达。
Proc Natl Acad Sci U S A. 1985 Aug;82(16):5505-9. doi: 10.1073/pnas.82.16.5505.
10
Organization and structure of the Qa genes of the major histocompatibility complex of the C3H mouse: implications for Qa function and class I evolution.C3H小鼠主要组织相容性复合体Qa基因的组织与结构:对Qa功能及I类基因进化的启示
EMBO J. 1989 Jun;8(6):1749-59. doi: 10.1002/j.1460-2075.1989.tb03568.x.

本文引用的文献

1
Antigenic profile of murine natural killer cells.小鼠自然杀伤细胞的抗原谱
J Immunol. 1980 Sep;125(3):1003-6.
2
Qa antigen expression on functional lymphoid, myeloid, and stem cells in adult mice.成年小鼠功能性淋巴细胞、髓细胞和干细胞上的Qa抗原表达。
J Immunol. 1980 Jun;124(6):2879-85.
3
Qa-2, H-2K, and H-2D alloantigens evolved from a common ancestral gene.Qa-2、H-2K和H-2D同种异体抗原由一个共同的祖先基因进化而来。
J Exp Med. 1981 May 1;153(5):1080-93. doi: 10.1084/jem.153.5.1080.
4
Further biochemical data on Qa-2.关于Qa-2的更多生化数据。
Immunogenetics. 1981;14(1-2):129-40. doi: 10.1007/BF00344306.
5
Qa-1-associated antigens. III. Distribution of Qa-1 region antigens on lymphoid subpopulations.Qa-1相关抗原。III. Qa-1区域抗原在淋巴亚群上的分布。
J Immunol. 1980 Dec;125(6):2597-603.
6
Notable diversity in peptide composition of murine H-2K and H-2D alloantigens.小鼠H-2K和H-2D同种异体抗原肽组成的显著差异。
Biochemistry. 1974 Jul 16;13(15):3174-8. doi: 10.1021/bi00712a027.
7
On the role of the H-2 histocompatibility complex in determining the specificity of cytotoxic effector cells sensitized against syngeneic trinitrophenyl-modified targets.关于H-2组织相容性复合体在确定针对同基因三硝基苯基修饰靶标的细胞毒性效应细胞特异性中的作用。
J Exp Med. 1975 Aug 1;142(2):403-18. doi: 10.1084/jem.142.2.403.
8
Histocompatibility-2 system in wild mice. V. Serologic analysis of sixteen B10.W congenic lines.野生小鼠的组织相容性-2系统。V. 16个B10.W同源近交系的血清学分析。
J Immunol. 1977 Dec;119(6):1903-11.
9
Molecular similarities between the Qa-2 alloantigen and other gene products of the 17th chromosome of the mouse.小鼠第17号染色体的Qa-2同种异体抗原与其他基因产物之间的分子相似性。
J Exp Med. 1977 Apr 1;145(4):1066-70. doi: 10.1084/jem.145.4.1066.
10
Qa-2 and Qa-3 antigens on lymphocyte subpopulations. I. Mitogen responsiveness.淋巴细胞亚群上的Qa - 2和Qa - 3抗原。I. 有丝分裂原反应性
J Immunol. 1978 Nov;121(5):1640-3.

Qa2亚区控制两种可被H-2非限制性细胞毒性T细胞识别的抗原的表达。

The Qa2 subregion controls the expression of two antigens recognized by H-2-unrestricted cytotoxic T cells.

作者信息

Forman J, Trial J, Tonkonogy S, Flaherty L

出版信息

J Exp Med. 1982 Mar 1;155(3):749-67. doi: 10.1084/jem.155.3.749.

DOI:10.1084/jem.155.3.749
PMID:6174664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2186634/
Abstract

B6.KI mice were immunized with spleen cells from B6.K2, a Qa2-subregion congenic strain. Cytotoxic T cells were generated that recognize two target antigens controlled by this region. One of the target antigens is Qa-2. This was demonstrated by the findings that pretreatment of target cells with monoclonal anti-Qa-2 antibody blocked lysis of target cells, and Qa-2 target antigens and serological determinants had a concordant distribution on a panel of B10.W (wild) mice. The gene controlling the Qa-2 target antigen is not polymorphic because B6.K2 and three strains of Qa-2(+) B10.W mice express the same antigens, as determined by a CTL cold target competition assay. Anti-Qa-2 CTL were H-2 unrestricted because effector cells lysed Qa-2(+) targets irrespective of their H-2 haplotype, including five B 10.W strains, and lysis was not inhibited by pretreating target cells with anti-H-2 sera. The Qa2 subregion does not act as a restricting locus for anti-minor-H antigen CTL. A second target antigen was detected that was associated with the expression of the Qa-5 determinant. However, CTL activity could not be blocked by pretreating target cells with monoclonal anti-Qa-5. Therefore, the CTL target antigen may be expressed on a Qa-5(-) molecule. Although the Qa-5 associated CTL specificity is only detected on H-2D(b) strains, it is unlikely that CTL recognition is H-2 restricted because anti-H-2(b) sera has no effect in blocking this reactivity. Qa-2 and H-2 class I antigens share a similar structure and serve as target antigens for unrestricted CTL. However, unlike class I H-2 genes, Qa-2 neither restricts antigen-specific CTL nor is polymorphie. Therefore, it is likely that Qa-2 and H-2 are derived from a common ancestral gene and have evolved to serve different functions.

摘要

用来自 Qa2 亚区同源品系 B6.K2 的脾细胞对 B6.KI 小鼠进行免疫。产生了识别该区域控制的两种靶抗原的细胞毒性 T 细胞。其中一种靶抗原是 Qa-2。这一点通过以下发现得以证明:用单克隆抗 Qa-2 抗体预处理靶细胞可阻断靶细胞的裂解,并且 Qa-2 靶抗原和血清学决定簇在一组 B10.W(野生)小鼠上具有一致的分布。控制 Qa-2 靶抗原的基因不是多态性的,因为通过细胞毒性 T 淋巴细胞冷靶竞争试验确定,B6.K2 和三株 Qa-2(+) B10.W 小鼠表达相同的抗原。抗 Qa-2 细胞毒性 T 淋巴细胞不受 H-2 限制,因为效应细胞可裂解 Qa-2(+)靶细胞,而不论其 H-2 单倍型如何,包括五株 B10.W 品系,并且用抗 H-2 血清预处理靶细胞不会抑制裂解。Qa2 亚区不作为抗次要组织相容性抗原细胞毒性 T 淋巴细胞的限制位点。检测到第二种与 Qa-5 决定簇表达相关的靶抗原。然而,用单克隆抗 Qa-5 预处理靶细胞并不能阻断细胞毒性 T 淋巴细胞活性。因此,细胞毒性 T 淋巴细胞靶抗原可能在 Qa-5(-)分子上表达。尽管与 Qa-5 相关的细胞毒性 T 淋巴细胞特异性仅在 H-2D(b)品系上检测到,但细胞毒性 T 淋巴细胞识别不太可能受 H-2 限制,因为抗 H-2(b)血清对阻断这种反应性没有作用。Qa-2 和 H-2 I 类抗原具有相似的结构,并作为不受限制的细胞毒性 T 淋巴细胞的靶抗原。然而,与 I 类 H-2 基因不同,Qa-2 既不限制抗原特异性细胞毒性 T 淋巴细胞,也不是多态性的。因此,Qa-2 和 H-2 很可能源自一个共同的祖先基因,并已进化以发挥不同的功能。