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1
Cellular immunity against Semliki Forest virus in mice.小鼠对塞姆利基森林病毒的细胞免疫
Infect Immun. 1979 Feb;23(2):213-8. doi: 10.1128/iai.23.2.213-218.1979.
2
Delayed-type hypersensitivity against Semliki Forest virus in mice.小鼠对Semliki森林病毒的迟发型超敏反应。
Infect Immun. 1979 Feb;23(2):219-23. doi: 10.1128/iai.23.2.219-223.1979.
3
Dimethyl dioctadecyl ammoniumbromide as an adjuvant for delayed type hypersensitivity and cellular immunity against Semliki Forest virus in mice.二甲基二十八烷基溴化铵作为小鼠迟发型超敏反应和针对塞姆利基森林病毒细胞免疫的佐剂
Arch Virol. 1980;65(3-4):211-7. doi: 10.1007/BF01314537.
4
Adoptive transfer of cross-protection among alphaviruses in mice requires allogeneic stimulation.小鼠中α病毒之间交叉保护的过继转移需要同种异体刺激。
Infect Immun. 1979 Jul;25(1):320-7. doi: 10.1128/iai.25.1.320-327.1979.
5
Preliminary evidence for cell-mediated immunity in cross-protection among group A arboviruses.
J Immunol. 1975 Feb;114(2 Pt 1):581-4.
6
Cytotoxic macrophages: a rapid nonspecific response to viral infection.细胞毒性巨噬细胞:对病毒感染的快速非特异性反应。
J Immunol. 1976 Dec;117(6):2067-72.
7
The responses of normal an athymic mice to infections by togaviruses: strain differentiation in active and adoptive immunization.正常小鼠和无胸腺小鼠对披膜病毒感染的反应:主动免疫和过继免疫中的毒株分化
J Gen Virol. 1980 Feb;46(2):255-65. doi: 10.1099/0022-1317-46-2-255.
8
Cross protection among togaviruses in nude mice and littermates.披膜病毒在裸鼠及其同窝小鼠中的交叉保护作用。
J Gen Virol. 1979 Oct;45(1):89-98. doi: 10.1099/0022-1317-45-1-89.
9
Adoptive transfer of immunity against virulent Semliki Forest virus with immune spleen cells from mice infected with avirulent Semliki Forest virus.用感染无毒力塞姆利基森林病毒的小鼠的免疫脾细胞进行针对强毒力塞姆利基森林病毒免疫的过继转移。
Arch Virol. 1986;91(1-2):83-92. doi: 10.1007/BF01316730.
10
In vitro heterologous cytotoxicity by T effector cells from mice immunized with Sindbis virus.用辛德毕斯病毒免疫的小鼠的T效应细胞的体外异源细胞毒性。
J Immunol. 1979 Oct;123(4):1763-6.

引用本文的文献

1
Simultaneous coinfection with influenza virus and an arbovirus impedes influenza-specific but not Semliki Forest virus-specific responses.流感病毒和虫媒病毒的同时感染会阻碍流感特异性反应,但不会阻碍塞姆利基森林病毒特异性反应。
Immunol Cell Biol. 2025 Apr;103(4):383-400. doi: 10.1111/imcb.70003. Epub 2025 Feb 19.
2
Pathogenesis of virus-induced demyelination.病毒诱导的脱髓鞘病变的发病机制。
Adv Virus Res. 1993;42:249-324. doi: 10.1016/s0065-3527(08)60087-1.
3
Dimethyl dioctadecyl ammoniumbromide as an adjuvant for delayed type hypersensitivity and cellular immunity against Semliki Forest virus in mice.二甲基二十八烷基溴化铵作为小鼠迟发型超敏反应和针对塞姆利基森林病毒细胞免疫的佐剂
Arch Virol. 1980;65(3-4):211-7. doi: 10.1007/BF01314537.
4
Delayed-type hypersensitivity in mice after infection with avirulent Semliki Forest virus. Brief report.
Arch Virol. 1983;78(1-2):115-8. doi: 10.1007/BF01310865.
5
Identification of distinct antigenic determinants on Semliki Forest virus by using monoclonal antibodies with different antiviral activities.通过使用具有不同抗病毒活性的单克隆抗体鉴定塞姆利基森林病毒上不同的抗原决定簇。
J Virol. 1984 Nov;52(2):575-82. doi: 10.1128/JVI.52.2.575-582.1984.
6
Adoptive transfer of immunity against virulent Semliki Forest virus with immune spleen cells from mice infected with avirulent Semliki Forest virus.用感染无毒力塞姆利基森林病毒的小鼠的免疫脾细胞进行针对强毒力塞姆利基森林病毒免疫的过继转移。
Arch Virol. 1986;91(1-2):83-92. doi: 10.1007/BF01316730.
7
Mechanisms of monoclonal antibody-mediated protection against virulent Semliki Forest virus.单克隆抗体介导的抗强毒株塞姆利基森林病毒保护机制
J Virol. 1985 May;54(2):546-51. doi: 10.1128/JVI.54.2.546-551.1985.
8
A delayed-type hypersensitivity-inducing T-cell epitope of Semliki Forest virus mediates effective T-helper activity for antibody production.塞姆利基森林病毒的一种迟发型超敏反应诱导性T细胞表位介导抗体产生的有效辅助性T细胞活性。
Immunology. 1992 Nov;77(3):322-9.

本文引用的文献

1
Infection patterns in mice of an avirulent and virulent strain of Semliki Forest virus.减毒和强毒株塞姆利基森林病毒在小鼠中的感染模式
Br J Exp Pathol. 1971 Dec;52(6):669-77.
2
The virulence of original and derived strains of Semliki forest virus for mice, guinea-pigs and rabbits.塞姆利基森林病毒原始株及衍生株对小鼠、豚鼠和兔子的毒力。
J Gen Virol. 1971 Aug;12(2):141-60. doi: 10.1099/0022-1317-12-2-141.
3
The mediator of cellular immunity. II. Migration of immunologically committed lymphocytes into inflammatory exudates.细胞免疫的介质。II. 免疫致敏淋巴细胞向炎性渗出物中的迁移。
J Exp Med. 1971 Feb 1;133(2):400-9. doi: 10.1084/jem.133.2.400.
4
Fluorescence-activated cell sorting of human T and B lymphocytes. II. Identification of the cell type responsible for interferon production and cell proliferation in response to mitogens.人T和B淋巴细胞的荧光激活细胞分选。II. 鉴定对有丝分裂原产生干扰素和细胞增殖反应的细胞类型。
Cell Immunol. 1974 Jun;12(3):407-21. doi: 10.1016/0008-8749(74)90097-5.
5
Quantitative studies of the inflammatory process in fatal viral meningoencephalitis.致命性病毒性脑膜脑炎炎症过程的定量研究。
Am J Pathol. 1973 Dec;73(3):607-22.
6
Investigations into yellow fever virus and other arboviruses in the northern regions of Kenya.对肯尼亚北部地区黄热病病毒及其他虫媒病毒的调查。
Bull World Health Organ. 1970;42(5):787-95.
7
Suppression of murine virus leukaemogenesis by thioglycollate, a bacteriological culture medium that affects macrophage peroxidase.巯基乙酸盐对小鼠病毒白血病发生的抑制作用,巯基乙酸盐是一种影响巨噬细胞过氧化物酶的细菌培养基。
Nature. 1975 May 22;255(5506):343-4. doi: 10.1038/255343a0.
8
Cytotoxic macrophages: a rapid nonspecific response to viral infection.细胞毒性巨噬细胞:对病毒感染的快速非特异性反应。
J Immunol. 1976 Dec;117(6):2067-72.
9
Increased spreading of macrophages from mice treated with interferon inducers.
Cell Immunol. 1977 Mar 1;29(1):86-95. doi: 10.1016/0008-8749(77)90277-5.
10
Interaction of mouse peritoneal macrophages with different arboviruses in vitro.小鼠腹腔巨噬细胞与不同虫媒病毒在体外的相互作用。
J Gen Virol. 1977 Feb;34(2):353-61. doi: 10.1099/0022-1317-34-2-353.

小鼠对塞姆利基森林病毒的细胞免疫

Cellular immunity against Semliki Forest virus in mice.

作者信息

Kraaijeveld C A, Harmsen M, Khader Boutahar-Trouw B

出版信息

Infect Immun. 1979 Feb;23(2):213-8. doi: 10.1128/iai.23.2.213-218.1979.

DOI:10.1128/iai.23.2.213-218.1979
PMID:311341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC414150/
Abstract

Intracutaneous immunization of BALB/c mice with purified inactivated Semliki Forest virus resulted in cellular immunity without detectable antibodies. The animals were protected against subcutaneous challenge, from which the challenge virus spreads slowly. After intraperitoneal challenge, which permits a rapid virus spread, the protection was marginal. Stimulation of the intraperitoneal cell population with thioglycolate before challenge resulted in complete protection. The protection could be transferred to normal mice with peripheral lymph node cells, but not with spleen cells. The course of the infection in immunized and normal mice was also studied. Semliki Forest virus does not multiply in peritoneal cells in vivo. In immunized mice part of the challenge virus in the peritoneal cavity was rapidly eliminated and viremia was reduced. After challenge, immunized mice produced less antibody than normal mice.

摘要

用纯化的灭活塞姆利基森林病毒对BALB/c小鼠进行皮内免疫,可诱导出细胞免疫,且未检测到抗体。这些动物受到保护,可抵御皮下攻击,皮下攻击的病毒传播缓慢。腹腔内攻击时,病毒传播迅速,保护作用微弱。攻击前用巯基乙酸盐刺激腹腔细胞群体可实现完全保护。这种保护作用可通过外周淋巴结细胞转移给正常小鼠,但不能通过脾细胞转移。还研究了免疫小鼠和正常小鼠的感染过程。塞姆利基森林病毒在体内不会在腹腔细胞中增殖。在免疫小鼠中,腹腔内的部分攻击病毒被迅速清除,病毒血症减轻。攻击后,免疫小鼠产生的抗体比正常小鼠少。