• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

印度内脏利什曼病中对γ干扰素加五价锑的反应

Response to interferon-gamma plus pentavalent antimony in Indian visceral leishmaniasis.

作者信息

Sundar S, Singh V P, Sharma S, Makharia M K, Murray H W

机构信息

Kala-Azar Medical Research Center, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.

出版信息

J Infect Dis. 1997 Oct;176(4):1117-9. doi: 10.1086/516526.

DOI:10.1086/516526
PMID:9333181
Abstract

One hundred fifty-six previously untreated Indian patients with visceral leishmaniasis were treated with pentavalent antimony (Sb) alone for 30 days (group A), Sb plus interferon-gamma (IFN-gamma) for 30 days (group B), or Sb plus IFN-gamma for 15 days (group C). The purpose was to show that IFN-gamma would increase the response to 30 days of Sb treatment and that short-course (15 days) combination therapy was as effective as 30 days of Sb alone. Six months after treatment, 36% of group A, 49% of group B, and 42% of group C patients were designated as definitively cured. The success rates for long-term responses to Sb alone (36%) and Sb plus IFN-gamma (49%) were unexpectedly low, and responses in groups A, B, and C were not significantly different. These results suggest that the beneficial effects of adjunctive IFN-gamma in visceral leishmaniasis may be limited in regions where this disseminated intracellular infection shows high-level resistance to Sb.

摘要

156名先前未经治疗的印度内脏利什曼病患者分别接受以下治疗:仅用五价锑(Sb)治疗30天(A组);Sb加干扰素-γ(IFN-γ)治疗30天(B组);或Sb加IFN-γ治疗15天(C组)。目的是证明IFN-γ会增强对30天Sb治疗的反应,并且短疗程(15天)联合治疗与仅用30天Sb治疗的效果相同。治疗6个月后,A组36%、B组49%和C组42%的患者被确定为完全治愈。仅用Sb(36%)和Sb加IFN-γ(49%)的长期反应成功率出乎意料地低,且A、B、C三组的反应无显著差异。这些结果表明,在这种播散性细胞内感染对Sb表现出高度耐药性的地区,辅助性IFN-γ在内脏利什曼病中的有益作用可能有限。

相似文献

1
Response to interferon-gamma plus pentavalent antimony in Indian visceral leishmaniasis.印度内脏利什曼病中对γ干扰素加五价锑的反应
J Infect Dis. 1997 Oct;176(4):1117-9. doi: 10.1086/516526.
2
Immunochemotherapy for a systemic intracellular infection: accelerated response using interferon-gamma in visceral leishmaniasis.用于全身性细胞内感染的免疫化疗:在内脏利什曼病中使用γ干扰素加速反应。
J Infect Dis. 1995 Apr;171(4):992-6. doi: 10.1093/infdis/171.4.992.
3
Treatment of visceral leishmaniasis with pentavalent antimony and interferon gamma.
N Engl J Med. 1990 Jan 4;322(1):16-21. doi: 10.1056/NEJM199001043220104.
4
Immunochemotherapy of visceral leishmaniasis: a pilot trial of sequential treatment with recombinant interferon-gamma and pentavalent antimony.
J Interferon Res. 1993 Feb;13(1):39-41. doi: 10.1089/jir.1993.13.39.
5
Immunochemotherapy for visceral leishmaniasis: a controlled pilot trial of antimony versus antimony plus interferon-gamma.
Am J Trop Med Hyg. 1993 May;48(5):666-9. doi: 10.4269/ajtmh.1993.48.666.
6
The role of interferon-gamma in the treatment of visceral and diffuse cutaneous leishmaniasis.γ干扰素在治疗内脏利什曼病和弥漫性皮肤利什曼病中的作用。
J Infect Dis. 1993 Mar;167 Suppl 1:S13-7. doi: 10.1093/infdis/167.supplement_1.s13.
7
Short term treatment of visceral leishmaniasis of the Old World with low dose interferon gamma and pentavalent antimony.低剂量干扰素γ与五价锑对旧大陆内脏利什曼病的短期治疗
Infection. 1993 Nov-Dec;21(6):362-6. doi: 10.1007/BF01728914.
8
Successful treatment of refractory visceral leishmaniasis in India using antimony plus interferon-gamma.在印度使用锑剂加γ-干扰素成功治疗难治性内脏利什曼病。
J Infect Dis. 1994 Sep;170(3):659-62. doi: 10.1093/infdis/170.3.659.
9
Response to chemotherapy in experimental visceral leishmaniasis: T cell-dependent but interferon-gamma- and interleukin-2-independent.实验性内脏利什曼病对化疗的反应:依赖T细胞,但不依赖干扰素-γ和白细胞介素-2 。
J Infect Dis. 1991 Mar;163(3):622-4. doi: 10.1093/infdis/163.3.622.
10
The use of recombinant gamma interferon associated with pentavalent antimony in therapy for visceral leishmaniasis.
Mem Inst Oswaldo Cruz. 1988 Nov;83 Suppl 1:376-7. doi: 10.1590/s0074-02761988000500028.

引用本文的文献

1
The story of elimination of visceral leishmaniasis (kala-azar) in India-Challenges towards sustainment.印度消除内脏利什曼病(黑热病)的历程——维持消除成果面临的挑战
PLoS Negl Trop Dis. 2025 Aug 19;19(8):e0013321. doi: 10.1371/journal.pntd.0013321. eCollection 2025 Aug.
2
Immunotherapy and immunochemotherapy in combating visceral leishmaniasis.免疫疗法和免疫化学疗法对抗内脏利什曼病
Front Med (Lausanne). 2023 May 17;10:1096458. doi: 10.3389/fmed.2023.1096458. eCollection 2023.
3
Evaluation of synergy between host and pathogen-directed therapies against intracellular Leishmania donovani.
评估针对细胞内杜氏利什曼原虫的宿主和病原体导向治疗的协同作用。
Int J Parasitol Drugs Drug Resist. 2019 Aug;10:125-132. doi: 10.1016/j.ijpddr.2019.08.004. Epub 2019 Aug 21.
4
Systematic Review of Host-Mediated Activity of Miltefosine in Leishmaniasis through Immunomodulation.米替福新通过免疫调节在利什曼病中宿主介导活性的系统评价。
Antimicrob Agents Chemother. 2019 Jun 24;63(7). doi: 10.1128/AAC.02507-18. Print 2019 Jul.
5
Combined neutralization of interferon gamma and tumor necrosis factor alpha induces IL-4 production but has no direct additive impact on parasite burden in splenic cultures of human visceral leishmaniasis.联合中和干扰素 γ 和肿瘤坏死因子 α 可诱导 IL-4 产生,但对内脏利什曼病患者脾培养物中的寄生虫负荷没有直接的附加影响。
PLoS One. 2018 Jun 28;13(6):e0199817. doi: 10.1371/journal.pone.0199817. eCollection 2018.
6
Immunomodulatory Therapy of Visceral Leishmaniasis in Human Immunodeficiency Virus-Coinfected Patients.人类免疫缺陷病毒合并感染患者内脏利什曼病的免疫调节治疗
Front Immunol. 2018 Jan 12;8:1943. doi: 10.3389/fimmu.2017.01943. eCollection 2017.
7
Chemotherapeutics of visceral leishmaniasis: present and future developments.内脏利什曼病的化疗药物:现状与未来发展
Parasitology. 2018 Apr;145(4):481-489. doi: 10.1017/S0031182017002116. Epub 2017 Dec 7.
8
Revisiting zoonotic human African trypanosomiasis control in Uganda.重新审视乌干达人畜共患非洲锥虫病的防控
J Public Health Policy. 2016 Feb;37(1):51-67. doi: 10.1057/jphp.2015.39. Epub 2015 Dec 3.
9
Host-mediated Leishmania donovani treatment using AR-12 encapsulated in acetalated dextran microparticles.使用封装在乙缩醛化葡聚糖微粒中的AR-12进行宿主介导的杜氏利什曼原虫治疗。
Int J Pharm. 2016 Feb 29;499(1-2):186-194. doi: 10.1016/j.ijpharm.2016.01.004. Epub 2016 Jan 5.
10
Leishmania specific CD4 T cells release IFNγ that limits parasite replication in patients with visceral leishmaniasis.利什曼原虫特异性CD4 T细胞释放γ干扰素,可限制内脏利什曼病患者体内寄生虫的复制。
PLoS Negl Trop Dis. 2014 Oct 2;8(10):e3198. doi: 10.1371/journal.pntd.0003198. eCollection 2014 Oct.