Bonilla-Abadía Fabio, Tobón Gabriel J, Cañas Carlos A
Division of Rheumatology, Department of Internal Medicine, Fundación Valle del Lili and ICESI University School of Medicine, Cali, Colombia ; Laboratory of Immunorheumatology, Carrera 98 N. 18-49, Cali, Colombia.
Arthritis. 2012;2012:670579. doi: 10.1155/2012/670579. Epub 2012 Nov 14.
Rheumatoid arthritis (RA) is a common autoimmune disease that affects all ethnic groups. Genetic factors, mainly HLA alleles, are highly associated with increased risk to develop RA. However, there are few available data about the role of these genetic polymorphisms in the prevalence or severity of RA in the Afrodescendant population, who have evolutionarily and by natural selection developed mutations that allowed them to acquire resistance to infectious diseases like malaria. Some of the mechanisms, by which this resistance was developed as a product of natural selection, are involved in different forms of immunological response, many of them of a well-known importance in the pathophysiology of RA. This paper focuses on presenting the known mechanisms of resistance to malaria and their possible contribution to the pathophysiology of RA, including "loss-of-function" mutations, lack of expression of chemokine receptors, decrease of immune complexes clearance by asplenia, or increase of immune reactivity mediated by B cells, among other mechanisms in this special group of patients.
类风湿性关节炎(RA)是一种影响所有种族群体的常见自身免疫性疾病。遗传因素,主要是HLA等位基因,与患RA风险增加高度相关。然而,关于这些基因多态性在非洲裔人群RA患病率或严重程度中的作用,可用数据很少。非洲裔人群通过进化和自然选择发生了突变,从而获得了对疟疾等传染病的抵抗力。作为自然选择产物而产生这种抵抗力的一些机制,参与了不同形式的免疫反应,其中许多在RA的病理生理学中具有众所周知的重要性。本文重点介绍对疟疾的已知抵抗机制及其对RA病理生理学的可能贡献,包括“功能丧失”突变、趋化因子受体表达缺失、脾脏缺失导致免疫复合物清除减少,或B细胞介导的免疫反应性增加等,这是该特殊患者群体中的其他机制。