This grant is aimed at discovering the etiology of endemic pemphigus foliaceus (PF), also known as Fogo Selvagem (FS) in rural Brazil. This epidermal-specific autoimmune disease is mediated by pathogenic IgG4 anti-desmoglein 1 (Dsg1) autoantibodies. In 1994, we identified the Amerindian Reservation of Limao Verde (LV), Brazil composed of ~1,400 individuals where the prevalence of FS was ~3%. Importantly, we have followed this population clinically and serologically for the last 18 years, identifying transitions from normal to FS in 12 individuals, and reported that exposure to blood feeding arthropods is a potential risk factor for FS. Moreover, the sera of patients with leishmaniasis, Chagas disease and onchocerciasis, where these insects are involved as carriers of parasites, possess anti-Dsg1 antibodies. Recently, we have shown that IgG4 anti-Dsg1 autoantibodies cross-react with conformational epitopes of the LJM11 yellow protein from the saliva of Lutzomyia longipalpis, the vector of leishmaniasis. The objective of this proposal is to determine how Dsg1 becomes the target of the immune system in FS and to identify the environmental antigen(s) that initiate the anti-self response. Based on previous studies, we hypothesize that salivary antigens from hematophagous insects are the source of sensitizing antigen in FS.
The aims of this grant will identify epitopes on Dsg1 and LJM11 that cross-react with IgG4 antibodies from FS patients and test whether these antibodies present in patient sera derive from na?ve B cells that bind foreign or self-antigens or both.
In Aim 1 we will determine the conformational epitopes bound by IgG4 anti-Dsg1 polyclonal antibodies from sera and B cells of FS patients on Dsg1(self) and LJM11(sand fly) antigens. Moreover, we shall test if murine anti-LJM11 antibodies, that bind human Dgs1, are pathogenic by passive transfer experiments.
In Aim 2 we shall generate IgG4 monoclonal antibodies (scFv) from FS B cells by phage display methods and select Dsg1 and LJM11 specific clones by panning procedures. These scFv antibodies will be tested for pathogenicity and used for more precise epitope mapping. Further, revertant monoclonal antibodies will be generated and tested for reactivity with Dsg1 and LJM11 in an effort to disclose the initial trigger of the IgG4 antibody response in FS.
Aim 3 and 4 are concerned with seroepidemiological studies in three cohorts and the population of Limao Verde. We shall continue searching for risk factors that may precipitate the IgG autoimmune response in normal subjects and the IgG4 in FS patients. The transition from normal to disease state will likely be uncovered on the follow up studies of the cohorts. At the completion of these novel studies we shall have a better understanding of how environmental antigens might trigger, in certain genetically predisposed individuals, an autoimmune IgG4 response that leads to skin diseases. In parallel, new epitope-specific immunoassays and potential novel therapeutic interventions may evolve from these studies.
The grant RO1 AR32599 is aimed at disclosing the etiology of a human autoimmune skin disease, pemphigus foliaceus, which is endemic in Brazil. At the completion of this application we will have a better understanding of how other human autoimmune diseases like lupus erythematosus, rheumatoid arthritis, thyroiditis, etc. evolve. Additionally, new diagnostic assays and potential therapeutic interventions will also be generated
|Evangelista, Flor; Roth, Aleeza J; Prisayanh, Phillip et al. (2018) Pathogenic IgG4 autoantibodies from endemic pemphigus foliaceus recognize a desmoglein-1 conformational epitope. J Autoimmun 89:171-185|
|Maldonado, Mike; Diaz, Luis A; Prisayanh, Phillip et al. (2017) Divergent Specificity Development of IgG1 and IgG4 Autoantibodies in Endemic Pemphigus Foliaceus (Fogo Selvagem). Immunohorizons 1:71-80|
|Boyden, Lynn M; Vincent, Nicholas G; Zhou, Jing et al. (2017) Mutations in KDSR Cause Recessive Progressive Symmetric Erythrokeratoderma. Am J Hum Genet 100:978-984|
|Li, Ning; Park, Moonhee; Xiao, Shengxiang et al. (2017) ER-to-Golgi blockade of nascent desmosomal cadherins in SERCA2-inhibited keratinocytes: Implications for Darier's disease. Traffic 18:232-241|
|Qian, Ye; Jeong, Joseph S; Ye, Jian et al. (2016) Overlapping IgG4 Responses to Self- and Environmental Antigens in Endemic Pemphigus Foliaceus. J Immunol 196:2041-50|
|Qian, Ye; Culton, Donna A; Jeong, Joseph S et al. (2016) Non-infectious environmental antigens as a trigger for the initiation of an autoimmune skin disease. Autoimmun Rev 15:923-30|
|Zuo, Yagang; Evangelista, Flor; Culton, Donna et al. (2016) IgG4 autoantibodies are inhibitory in the autoimmune disease bullous pemphigoid. J Autoimmun 73:111-9|
|Culton, Donna A; McCray, Suzanne K; Park, Moonhee et al. (2015) Mucosal pemphigus vulgaris anti-Dsg3 IgG is pathogenic to the oral mucosa of humanized Dsg3 mice. J Invest Dermatol 135:1590-1597|
|Aoki, Valeria; Rivitti, Evandro A; Diaz, Luis A et al. (2015) Update on fogo selvagem, an endemic form of pemphigus foliaceus. J Dermatol 42:18-26|
|Qian, Ye; Jeong, Joseph S; Abdeladhim, Maha et al. (2015) IgE anti-LJM11 sand fly salivary antigen may herald the onset of fogo selvagem in endemic Brazilian regions. J Invest Dermatol 135:913-915|
Showing the most recent 10 out of 138 publications