Zobrazeno 1 - 10
of 1 686
pro vyhledávání: '"immunoglobulin G4"'
Immunoglobulin G4-related pancreatitis presenting as an obstructive pancreatic mass in a Latino male
Publikováno v:
Journal of Family and Community Medicine, Vol 31, Iss 4, Pp 351-354 (2024)
Immunoglobulin G4-related disease (IgG4-RD) is a localized or diffuse autoimmune fibro-inflammatory condition that can affect any organ. The literature is sparse on IgG4-RD in the Latino population. This is a case report of a Latino male diagnosed wi
Externí odkaz:
https://doaj.org/article/c7be1389f66342e7901d64f06006b60f
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Primary Sjögren’s syndrome (pSS) is an autoimmune disease, with B cell hyperactivation and autoantibody production as its immunological hallmarks. Although the distinction between immunoglobulin G4-related disease (IgG4-RD) and pSS, based on the p
Externí odkaz:
https://doaj.org/article/7f0298a036344e3b96f6d6fdcc40cf52
Autor:
Mikolaj Raszek, David Cowley, Elrashdy M. Redwan, Vladimir N. Uversky, Alberto Rubio-Casillas
Publikováno v:
Exploration of Immunology, Vol 4, Iss 2, Pp 267-284 (2024)
Repeated inoculation with messenger RNA (mRNA) vaccines elicits immunoglobulin G4 (IgG4) antibody production. Such an increase in the concentration of specific and non-specific IgG4 antibodies allows the growth of some types of cancer by blocking the
Externí odkaz:
https://doaj.org/article/cd9a494398f04954b8784bc0e34ae803
Publikováno v:
Journal of Oral Microbiology, Vol 16, Iss 1 (2024)
Background The association of chronic sclerosing sialadenitis and IgG4-related disease (IgG4-RD) has resulted in the more frequent identification of IgG4-positivity in submandibular gland inflammations, also uncovering IgG4 overexpression in nonspeci
Externí odkaz:
https://doaj.org/article/9cdc4c584bcb4153be8b13fc2bb9a81d
Autor:
Noora Keski-Säntti, Elin Waltimo, Antti Mäkitie, Jaana Hagström, Maria Söderlund-Venermo, Timo Atula, Caj Haglund, Saku T. Sinkkonen, Maria Jauhiainen
Publikováno v:
Journal of Oral Microbiology, Vol 16, Iss 1 (2024)
Background The etiology behind different types of chronic sialadenitis (CS), some of which exhibit IgG4 overexpression, is unknown. Further, IgG4-related disease (IgG4-RD) commonly affects the submandibular gland, but its relationship to IgG4-overexp
Externí odkaz:
https://doaj.org/article/5976656897cd41f4ad293e3c91b1469b
Publikováno v:
Open Life Sciences, Vol 18, Iss 1, Pp 235-59 (2023)
To evaluate the clinical significance of detecting serum IgG4 and the IgG4/IgG ratio in patients with thyroid-associated ophthalmopathy (TAO) and to explore whether high serum IgG4 levels and the IgG4/IgG ratio are associated with the severity and ac
Externí odkaz:
https://doaj.org/article/a299515da43145eaaff9e35876b0e166
Autor:
Phattharaphon Wongphutorn, Chanika Worasith, Kulthida Y. Kopolrat, Chutima Homwong, Jiraporn Sithithaworn, Chatanun Eamudomkarn, Anchalee Techasen, Patcharaporn Tippayawat, Opal Pitaksakurat, Nuttanan Hongsrichan, Thomas Crellen, Paiboon Sithithaworn
Publikováno v:
Parasites & Vectors, Vol 16, Iss 1, Pp 1-12 (2023)
Abstract Background Detection of parasite-specific IgG in urine is a sensitive method for diagnosis of strongyloidiasis and gives similar accuracy to serum IgG. However, there are no data concerning detection of IgG subclass in urine. To further expl
Externí odkaz:
https://doaj.org/article/8af99cef948c46fc85fae7e512b0056a
Autor:
Ahmet Parlak, Christian-Andreas Mueller, Kay W. Nolte, Tobias P. Schmidt, Ulf Bertram, Hans Clusmann, Christian Blume
Publikováno v:
Brain and Spine, Vol 4, Iss , Pp 103325- (2024)
Introduction: IgG4-related disease is an immune-mediated condition characterized by tissue infiltration of IgG4-positive plasma cells. Involvement of the spinal meninges results in hypertrophic spinal pachymeningitis (HSP), causing spinal cord and ne
Externí odkaz:
https://doaj.org/article/b976a179a64d423aa2ebb9549b7aef22
Autor:
Shigeyuki Tahara, Robert Yoshiyuki Osamura, Yujiro Hattori, Eitaro Ishisaka, Chie Inomoto, Hitoshi Sugihara, Akira Teramoto, Akio Morita
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Some patients develop immunoglobulin G4 (IgG4)-related hypophysitis associated with systemic diseases. More than 30 cases of IgG4-related hypophysitis have been reported. However, biopsy has rarely been performed in these patients
Externí odkaz:
https://doaj.org/article/dbc3b588805249798ee755d9a3b975e3
Autor:
Aoi Koshida, Shigehiro Karashima, Kohei Ogura, Yuna Miyajima, Kazuhiro Ogai, Ren Mizoguchi, Yasuo Ikagawa, Satoshi Hara, Ichiro Mizushima, Hiroshi Fujii, Mitsuhiro Kawano, Hiromasa Tsujiguchi, Akinori Hara, Hiroyuki Nakamura, Shigefumi Okamoto
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2023)
IntroductionImmunoglobulin G4 (IgG4) is a member of the human immunoglobulin G (IgG) subclass, a protein involved in immunity to pathogens and the body’s resistance system. IgG4-related diseases (IgG4-RD) are intractable diseases in which IgG4 leve
Externí odkaz:
https://doaj.org/article/69dd751402ef4e20afefe22c05407f5a