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慢性恰加斯病患者体内针对受体酪氨酸激酶TrkA、TrkB和TrkC的自身抗体。

Auto-antibodies to receptor tyrosine kinases TrkA, TrkB and TrkC in patients with chronic Chagas' disease.

作者信息

Lu B, Petrola Z, Luquetti A O, PereiraPerrin M

机构信息

Department of Pathology, Parasitology Research Center, Tufts University School of Medicine, Boston, MA 02111, USA.

出版信息

Scand J Immunol. 2008 Jun;67(6):603-9. doi: 10.1111/j.1365-3083.2008.02102.x. Epub 2008 Apr 10.

Abstract

The Chagas' disease parasite Trypanosoma cruzi promotes survival and differentiation of neurones by binding and activating nerve growth factor (NGF) receptor TrkA. The functional mimic of NGF in T. cruzi is a surface-bound and shed immunogenic protein [neurotrophic factor/trans-sialidase (TS)], which raised the possibility that immune response to T. cruzi in general and to neurotrophic factor/TS in particular leads to loss of immunological tolerance to host NGF and/or the NGF-binding partner TrkA. In testing this hypothesis, we found that sera of individuals with chronic Chagas' disease bear unique IgG2 autoantibodies that bind TrkA and TrkA family members TrkB and TrkC (ATA). Binding of ATA to Trk receptors is specific because the autoantibodies did not cross-react with five other growth factor receptors, NGF and other neurotrophins, and T. cruzi. Thus, individuals with chronic Chagas' disease produce unique antibodies that react with pan-Trk receptors, one of which (TrkA) T. cruzi exploits to inhibit host cell apoptosis and to promote cellular invasion.

摘要

恰加斯病寄生虫克氏锥虫通过结合并激活神经生长因子(NGF)受体TrkA来促进神经元的存活和分化。克氏锥虫中NGF的功能模拟物是一种表面结合且可脱落的免疫原性蛋白[神经营养因子/转唾液酸酶(TS)],这增加了一种可能性,即一般针对克氏锥虫,特别是针对神经营养因子/TS的免疫反应会导致对宿主NGF和/或NGF结合伴侣TrkA的免疫耐受性丧失。在验证这一假设时,我们发现慢性恰加斯病患者的血清中含有独特的IgG2自身抗体,这些抗体可结合TrkA以及TrkA家族成员TrkB和TrkC(ATA)。ATA与Trk受体的结合具有特异性,因为这些自身抗体不会与其他五种生长因子受体、NGF和其他神经营养因子以及克氏锥虫发生交叉反应。因此,慢性恰加斯病患者会产生与泛Trk受体发生反应的独特抗体,其中一种(TrkA)被克氏锥虫利用来抑制宿主细胞凋亡并促进细胞侵袭。

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