دورية أكاديمية

Autoreactivity to Glucose Regulated Protein 78 Links Emphysema and Osteoporosis in Smokers

التفاصيل البيبلوغرافية
العنوان: Autoreactivity to Glucose Regulated Protein 78 Links Emphysema and Osteoporosis in Smokers
المؤلفون: Bon, Jessica, Kahloon, Rehan, Zhang, Yingze, Xue, Jianmin, Fuhrman, Carl R., Tan, Jiangning, Burger, Mathew, Kass, Daniel J., Csizmadia, Eva, Otterbein, Leo, Chandra, Divay, Bhargava, Arpit, Pilewski, Joseph M., Roodman, G. David, Sciurba, Frank C., Duncan, Steven R.
المصدر: Bon, J., R. Kahloon, Y. Zhang, J. Xue, C. R. Fuhrman, J. Tan, M. Burger, et al. 2014. “Autoreactivity to Glucose Regulated Protein 78 Links Emphysema and Osteoporosis in Smokers.” PLoS ONE 9 (9): e105066. doi:10.1371/journal.pone.0105066. http://dx.doi.org/10.1371/journal.pone.0105066Test.
بيانات النشر: Public Library of Science, 2014.
سنة النشر: 2014
المجموعة: HMS Scholarly Articles
مصطلحات موضوعية: Biology and Life Sciences, Immunology, Clinical Immunology, Autoimmune Diseases, Medicine and Health Sciences, Pulmonology, Chronic Obstructive Pulmonary Disease
الوصف: Rationale: Emphysema and osteoporosis are epidemiologically associated diseases of cigarette smokers. The causal mechanism(s) linking these illnesses is unknown. We hypothesized autoimmune responses may be involved in both disorders. Objectives: To discover an antigen-specific autoimmune response associated with both emphysema and osteoporosis among smokers. Methods: Replicate nonbiased discovery assays indicated that autoimmunity to glucose regulated protein 78 (GRP78), an endoplasmic reticulum chaperone and cell surface signaling receptor, is present in many smokers. Subject assessments included spirometry, chest CT scans, dual x-ray absorptiometry, and immunoblots for anti-GRP78 IgG. Anti-GRP78 autoantibodies were isolated from patient plasma by affinity chromatography, leukocyte functions assessed by flow cytometry, and soluble metabolites and mediators measured by immunoassays. Measurements and Main Results Circulating anti-GRP78 IgG autoantibodies were detected in plasma specimens from 86 (32%) of the 265 smoking subjects. Anti-GRP78 autoantibodies were singularly prevalent among subjects with radiographic emphysema (OR 3.1, 95%CI 1.7–5.7, p = 0.003). Anti-GRP78 autoantibodies were also associated with osteoporosis (OR 4.7, 95%CI 1.7–13.3, p = 0.002), and increased circulating bone metabolites (p = 0.006). Among emphysematous subjects, GRP78 protein was an autoantigen of CD4 T-cells, stimulating lymphocyte proliferation (p = 0.0002) and IFN-gamma production (p = 0.03). Patient-derived anti-GRP78 autoantibodies had avidities for osteoclasts and macrophages, and increased macrophage NFkB phosphorylation (p = 0.005) and productions of IL-8, CCL-2, and MMP9 (p = 0.005, 0.007, 0.03, respectively). Conclusions: Humoral and cellular GRP78 autoimmune responses in smokers have numerous biologically-relevant pro-inflammatory and other deleterious actions, and are associated with emphysema and osteoporosis. These findings may have relevance for the pathogenesis of smoking-associated diseases, and development of biomarker immunoassays and/or novel treatments for these disorders.
نوع الوثيقة: Journal Article
اللغة: English
تدمد: 1932-6203
العلاقة: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162538/pdfTest/; PLoS ONE
DOI: 10.1371/journal.pone.0105066
الوصول الحر: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12987327Test
رقم الانضمام: edshld.1.12987327
قاعدة البيانات: Digital Access to Scholarship at Harvard (DASH)
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0105066