Suppr超能文献

那他珠单抗与进行性多灶性白质脑病:致病因素有哪些,能否避免?

Natalizumab and progressive multifocal leukoencephalopathy: what are the causal factors and can it be avoided?

作者信息

Warnke Clemens, Menge Til, Hartung Hans-Peter, Racke Michael K, Cravens Petra D, Bennett Jeffrey L, Frohman Elliot M, Greenberg Benjamin M, Zamvil Scott S, Gold Ralf, Hemmer Bernhard, Kieseier Bernd C, Stüve Olaf

机构信息

Neurology Section, VA North Texas Health Care System, Medical Service, 4500 S Lancaster Rd, Dallas, TX 75216, USA.

出版信息

Arch Neurol. 2010 Aug;67(8):923-30. doi: 10.1001/archneurol.2010.161.

Abstract

Natalizumab (Tysabri) was the first monoclonal antibody approved for the treatment of relapsing forms of multiple sclerosis (MS). After its initial approval, 3 patients undergoing natalizumab therapy in combination with other immunoregulatory and immunosuppressive agents were diagnosed with progressive multifocal leukoencephalopathy (PML). The agent was later reapproved and its use restricted to monotherapy in patients with relapsing forms of MS. Since reapproval in 2006, additional cases of PML were reported in patients with MS receiving natalizumab monotherapy. Thus, there is currently no convincing evidence that natalizumab-associated PML is restricted to combination therapy with other disease-modifying or immunosuppressive agents. In addition, recent data indicate that risk of PML might increase beyond 24 months of treatment.

摘要

那他珠单抗(泰萨比)是首个被批准用于治疗复发型多发性硬化症(MS)的单克隆抗体。在其首次获批后,3名接受那他珠单抗治疗并联合其他免疫调节和免疫抑制药物的患者被诊断出患有进行性多灶性白质脑病(PML)。该药物后来再次获批,其使用仅限于复发型MS患者的单一疗法。自2006年再次获批以来,接受那他珠单抗单一疗法的MS患者中又报告了多例PML病例。因此,目前没有令人信服的证据表明与那他珠单抗相关的PML仅限于与其他疾病改善或免疫抑制药物联合治疗。此外,最近的数据表明,PML的风险可能在治疗超过24个月后增加。

相似文献

3
The link between VLA-4 and JC virus reactivation.
Expert Rev Clin Immunol. 2012 Jan;8(1):63-72. doi: 10.1586/eci.11.85.
5
Progressive multifocal leukoencephalopathy and natalizumab.
J Neurol. 2011 Nov;258(11):1920-8. doi: 10.1007/s00415-011-6116-8. Epub 2011 Jun 7.
6
Practical Clinical Guidelines for Natalizumab Treatment in Patients With Relapsing Multiple Sclerosis.
J Infus Nurs. 2023;46(6):347-359. doi: 10.1097/NAN.0000000000000519.
7
Therapeutic uses of anti-α4-integrin (anti-VLA-4) antibodies in multiple sclerosis.
Int Immunol. 2015 Jan;27(1):47-53. doi: 10.1093/intimm/dxu096. Epub 2014 Oct 17.
8
Multiple sclerosis, natalizumab therapy, and progressive multifocal leukoencephalopathy.
Curr Opin Neurol. 2006 Aug;19(4):341-9. doi: 10.1097/01.wco.0000236612.66839.a2.

引用本文的文献

1
Understanding the molecular mechanisms of anti-trafficking therapies and their clinical relevance in inflammatory bowel disease.
Mucosal Immunol. 2023 Dec;16(6):859-870. doi: 10.1016/j.mucimm.2023.08.001. Epub 2023 Sep 3.
2
Progressive Multifocal Leukoencephalopathy: Pathogenesis, Diagnostic Tools, and Potential Biomarkers of Response to Therapy.
Neurology. 2023 Oct 17;101(16):700-713. doi: 10.1212/WNL.0000000000207622. Epub 2023 Jul 24.
4
Transcriptomic and clonal characterization of T cells in the human central nervous system.
Sci Immunol. 2020 Sep 18;5(51). doi: 10.1126/sciimmunol.abb8786.
5
Role of Viruses in the Pathogenesis of Multiple Sclerosis.
Viruses. 2020 Jun 13;12(6):643. doi: 10.3390/v12060643.
6
Non-Invasive Delivery of Therapeutics into the Brain: The Potential of Aptamers for Targeted Delivery.
Biomedicines. 2020 May 14;8(5):120. doi: 10.3390/biomedicines8050120.
8
Maneuvering Clinical Pathways for Crohn's Disease.
Curr Gastroenterol Rep. 2019 Apr 23;21(5):20. doi: 10.1007/s11894-019-0687-4.
9
Age-Associated Changes in the Immune System and Blood⁻Brain Barrier Functions.
Int J Mol Sci. 2019 Apr 2;20(7):1632. doi: 10.3390/ijms20071632.
10
Frontline Science: Buprenorphine decreases CCL2-mediated migration of CD14 CD16 monocytes.
J Leukoc Biol. 2018 Dec;104(6):1049-1059. doi: 10.1002/JLB.3HI0118-015R. Epub 2018 May 23.

本文引用的文献

1
Identification and characterization of mefloquine efficacy against JC virus in vitro.
Antimicrob Agents Chemother. 2009 May;53(5):1840-9. doi: 10.1128/AAC.01614-08. Epub 2009 Mar 2.
3
Effect of plasma exchange in accelerating natalizumab clearance and restoring leukocyte function.
Neurology. 2009 Feb 3;72(5):402-9. doi: 10.1212/01.wnl.0000341766.59028.9d.
4
Steroids for PML-IRIS: a double-edged sword?
Neurology. 2009 Apr 28;72(17):1454-5. doi: 10.1212/01.wnl.0000343735.44983.5e. Epub 2009 Jan 14.
5
PML-IRIS in patients with HIV infection: clinical manifestations and treatment with steroids.
Neurology. 2009 Apr 28;72(17):1458-64. doi: 10.1212/01.wnl.0000343510.08643.74. Epub 2009 Jan 7.
6
Response to Linberg et al. Natalizumab alters transcriptional expression profiles of blood cell subpopulations of multiple sclerosis patients.
J Neuroimmunol. 2008 Nov 15;204(1-2):155-6; author reply 157. doi: 10.1016/j.jneuroim.2008.05.007.
7
New cases of progressive multifocal leukoencephalopathy after treatment with natalizumab.
Lancet Neurol. 2009 Jan;8(1):28-31. doi: 10.1016/S1474-4422(08)70281-3.
8
Immunologic, clinical, and radiologic status 14 months after cessation of natalizumab therapy.
Neurology. 2009 Feb 3;72(5):396-401. doi: 10.1212/01.wnl.0000327341.89587.76. Epub 2008 Nov 5.
9
Decrease in the numbers of dendritic cells and CD4+ T cells in cerebral perivascular spaces due to natalizumab.
Arch Neurol. 2008 Dec;65(12):1596-603. doi: 10.1001/archneur.65.12.noc80051. Epub 2008 Oct 13.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验