Zobrazeno 1 - 10
of 370
pro vyhledávání: '"Jiri Litzman"'
Autor:
Julie Stichova, Peter Slanina, Zita Chovancova, Jan Baros, Marek Litzman, Jiri Litzman, Marcela Vlkova
Publikováno v:
Frontiers in Allergy, Vol 5 (2024)
BackgroundPrevious research showed that the intracellular complement system, with CD46 as its central molecule, regulates the Th1 response associated with IFN-γ production and transition to a type 1 regulatory response (Tr1) characterized by IL-10 p
Externí odkaz:
https://doaj.org/article/a939423bc67b4332b988b74dd813a23a
Autor:
Ildikó Tar, Márta Szegedi, Ewa Krasuska-Sławińska, Edyta Heropolitańska-Pliszka, Ewa A. Bernatowska, Elif Öncü, Sevgi Keles, Sukru N. Guner, Ismail Reisli, Nevena Gesheva, Elissaveta Naumova, Lydie Izakovicova-Holla, Jiri Litzman, Igor Savchak, Larysa Kostyuchenko, Melinda Erdős
Publikováno v:
Central European Journal of Immunology, Vol 48, Iss 3, Pp 228-236 (2023)
Autosomal dominant hyper-IgE syndrome (AD-HIES) is an inborn error of immunity (IEI) caused by a dominant-negative mutation in the signal transducer and activator of transcription 3 (STAT 3). This disease is characterized by chronic eczematoid dermat
Externí odkaz:
https://doaj.org/article/c82a97b04920449189b05edd75f8ff55
Autor:
Máté Krausz, Noriko Mitsuiki, Valeria Falcone, Johanna Komp, Sara Posadas-Cantera, Hanns-Martin Lorenz, Jiri Litzman, Daniel Wolff, Maria Kanariou, Anita Heinkele, Carsten Speckmann, Georg Häcker, Hartmut Hengel, Laura Gámez-Díaz, Bodo Grimbacher
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/4811e267db8b4a0f951d41d027cdeb75
Autor:
Máté Krausz, Noriko Mitsuiki, Valeria Falcone, Johanna Komp, Sara Posadas-Cantera, Hanns-Martin Lorenz, Jiri Litzman, Daniel Wolff, Maria Kanariou, Anita Heinkele, Carsten Speckmann, Georg Häcker, Hartmut Hengel, Laura Gámez-Díaz, Bodo Grimbacher
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
PurposeHeterozygous mutations in CTLA4 lead to an inborn error of immunity characterized by immune dysregulation and immunodeficiency, known as CTLA-4 insufficiency. Cohort studies on CTLA4 mutation carriers showed a reduced penetrance (around 70%) a
Externí odkaz:
https://doaj.org/article/64f0ae1228b94a4eaeab35fff84eeb9a
Autor:
Tomas Milota, Marta Sobotkova, Jitka Smetanova, Marketa Bloomfield, Jana Vydlakova, Zita Chovancova, Jiri Litzman, Roman Hakl, Jiri Novak, Ivana Malkusova, Jana Hanzlikova, Dalibor Jilek, Beata Hutyrova, Vitezslav Novak, Irena Krcmova, Anna Sediva, Pavlina Kralickova
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Despite the progress in the understanding how COVID-19 infection may impact immunocompromised patients, the data on inborn errors of immunity (IEI) remain limited and ambiguous. Therefore, we examined the risk of severe infection course and hospital
Externí odkaz:
https://doaj.org/article/c9ffc8f2d5064127a039c58055a12895
Publikováno v:
Central European Journal of Immunology, Vol 42, Iss 3, Pp 244-251 (2017)
Introduction : Previous studies showed that several lymphocyte abnormalities seen in the most frequent symptomatic immunoglobulin deficiency, common variable immunodeficiency (CVID), were also observed in a genetically related asymptomatic disorder
Externí odkaz:
https://doaj.org/article/9f59517b08854d90b2b0ba016d3f72ad
Autor:
Renata Formankova, Veronika Kanderova, Marketa Rackova, Michael Svaton, Tomas Brdicka, Petr Riha, Petra Keslova, Ester Mejstrikova, Marketa Zaliova, Tomas Freiberger, Hana Grombirikova, Zuzana Zemanova, Marcela Vlkova, Filip Fencl, Ivana Copova, Jiri Bronsky, Petr Jabandziev, Petr Sedlacek, Jana Soukalova, Ondrej Zapletal, Jan Stary, Jan Trka, Tomas Kalina, Karolina Skvarova Kramarzova, Eva Hlavackova, Jiri Litzman, Eva Fronkova
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Mutations in the Sterile alpha motif domain containing 9 (SAMD9) gene have been described in patients with severe multisystem disorder, MIRAGE syndrome, but also in patients with bone marrow (BM) failure in the absence of other systemic symptoms. The
Externí odkaz:
https://doaj.org/article/bd4b5e4e6b0447a18fa5370f40186de9
Autor:
Pavlina Kralickova, Tomas Milota, Jiri Litzman, Ivana Malkusova, Dalibor Jilek, Jitka Petanova, Jana Vydlakova, Alena Zimulova, Eva Fronkova, Michael Svaton, Veronika Kanderova, Marketa Bloomfield, Zuzana Parackova, Adam Klocperk, Jiri Haviger, Tomas Kalina, Anna Sediva
Publikováno v:
Frontiers in Immunology, Vol 9 (2019)
Background: Common variable immunodeficiency disorder (CVID) is one of the most frequent inborn errors of immunity, increased occurrence of malignancies, particularly lymphomas, and gastric cancers, has long been noted among CVID patients. Multifacto
Externí odkaz:
https://doaj.org/article/645a1784924243fea1af507d9f4913e7
Autor:
Tereza Grymova, Marcela Vlkova, Premysl Soucek, Roman Hakl, Jana Nechvatalova, Peter Slanina, Julie Stichova, Jiri Litzman, Tomas Freiberger
Publikováno v:
Mediators of Inflammation, Vol 2019 (2019)
Neutrophils impact on processes preceding the formation of bradykinin, a major swelling mediator in hereditary angioedema (HAE), yet their potential role in HAE pathogenesis has not been sufficiently studied. We assessed the relative mRNA expression
Externí odkaz:
https://doaj.org/article/a2a35a4c26974bf78115c9d22cf318de
Autor:
Nina K. Serwas, Jakob Huemer, Régis Dieckmann, Ester Mejstrikova, Wojciech Garncarz, Jiri Litzman, Birgit Hoeger, Ondrej Zapletal, Ales Janda, Keiryn L. Bennett, Renate Kain, Dontscho Kerjaschky, Kaan Boztug
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Specific granule deficiency (SGD) is a rare disorder characterized by abnormal neutrophils evidenced by reduced granules, absence of granule proteins, and atypical bilobed nuclei. Mutations in CCAAT/enhancer-binding protein-ε (CEBPE) are one molecul
Externí odkaz:
https://doaj.org/article/8187cf6d031441d6985970193b8a4647