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Is Gulf War Syndrome an autoimmune disorder of endogenous neuropeptides, exogenous sandfly maxadilan and molecular mimicry?

机译:海湾战争综合症是内源性神经肽,外源性沙蝇maxadilan和分子模拟的自身免疫性疾病吗?

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Gulf War Syndrome (GWS) remains a contentious diagnosis with conflicting laboratory investigation and lack of a biologically plausible aetiology. This paper discusses the potential role of maxadilan, a potent sandfly vasoactive peptide, in causing autoimmune responses in susceptible individuals through possible molecular mimicry with pituitary adenylate cyclase activating polypeptide (PACAP) and the PAC1R receptor. Gulf War Syndrome may share some causative pathology with Chronic Fatigue Syndrome (CFS), a disorder characterised by prolonged fatigue and debility mostly associated with post-infection sequelae although ongoing infection is unproven. Immunological aberration associated with an expanding group of vasoactive neuropeptides in the context of molecular mimicry and inappropriate immunological memory has been recently raised as possible cause of CFS. Vasoactive neuropeptides act as hormones, neurotransmitters, immune modulators and neurotrophes. They are readily catalysed to small peptide fragments. They and their binding sites are immunogenic and are known to be associated with a range of autoimmune conditions. Maxadilan, while not sharing substantial sequence homology with PACAP is a known agonist of the PACAP specific receptor (PAC1R) and therefore emulates these functions. Moreover a specific amino acid sequence peptide deletion within maxadilan converts it to a PACAP receptor antagonist raising the possibility of this substance provoking a CFS like response in humans exposed to it. This paper describes a biologically plausible mechanism for the development of a GWS-like chronic fatigue state based on loss of immunological tolerance to the vasoactive neuropeptide PACAP or its receptor following bites of the sandfly Phlebotomus papatasi and injection of the vasodilator peptide maxadilan. Exacerbation of this autoimmune response as a consequence of recent or simultaneous multiple vaccination exposures deserves further investigation. While the possible association between the relatively recently discovered vasoactive neuropeptides and chronic fatigue conditions has only recently been reported in the literature, this paper explores links for further research into GWS and CFS.
机译:海湾战争综合症(GWS)仍然是一项有争议的诊断,实验室研究冲突且缺乏生物学上合理的病因。本文讨论了一种强效的fly蝇血管活性肽maxadilan在可能的分子垂体腺苷酸环化酶激活多肽(PACAP)和PAC1R受体的分子模拟中引起自身免疫应答中的潜在作用。海湾战争综合症可能与慢性疲劳综合症(CFS)共享某些病因,这种疾病的特点是疲劳和残疾时间延长,通常与感染后遗症有关,尽管目前的感染尚无证。最近已经提出了在分子模拟和不适当的免疫记忆的情况下与不断增加的血管活性神经肽相关的免疫学异常,这可能是CFS的原因。血管活性神经肽可作为激素,神经递质,免疫调节剂和神经碱。它们易于催化成小的肽片段。它们和它们的结合位点是免疫原性的,并且已知与一系列自身免疫疾病有关。 Maxadilan虽然与PACAP没有基本的序列同源性,但却是PACAP特异性受体(PAC1R)的已知激动剂,因此可模拟这些功能。此外,maxadilan中特定氨基酸序列肽的缺失将其转变为PACAP受体拮抗剂,从而增加了该物质在暴露于其的人体中引起CFS样反应的可能性。本文描述了一种生物学上合理的机制,可用于开发类似GWS的慢性疲劳状态,这是由于在咬住fly蝇白粉病和注射血管舒张剂肽maxadilan之后丧失了对血管活性神经肽PACAP或其受体的免疫耐受性。由于近期或同时进行多次疫苗接种,这种自身免疫反应的加剧值得进一步研究。虽然相对较新发现的血管活性神经肽和慢性疲劳状况之间的关联可能只是最近才在文献中报道,但本文还是探索了对GWS和CFS进行进一步研究的联系。

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