EGG, D., I. C. RUMP, N. MITSUIKI, J. ROJAS-RESTREPO, M. E. MACCARI, C. SCHWAB, A. GABRYSCH, K. WARNATZ, S. GOLDACKER, V. PATIÑO, D. WOLFF, S. OKADA, S. HAYAKAWA, Y. SHIKAMA, K. KANDA, K. IMAI, M. SOTOMATSU, M. KUWASHIMA, T. KAMIYA, T. MORIO, K. MATSUMOTO, T. MORI, Y. YOSHIMOTO, I. DYBEDAL, M. KANARIOU, Z. Y. KUCUK, H. CHAPDELAINE, L. PETRUZELKOVA, H. M. LORENZ, K. E. SULLIVAN, J. HEIMALL, M. MOUTSCHEN, Jiří LITZMAN, M. RECHER, M. H. ALBERT, F. HAUCK, S. SENEVIRATNE, J. PACHLOPNIK SCHMID, A. KOLIOS, G. UNGLIK, C. KLEMANN, S. SNAPPER, L. GIULINO-ROTH, Michael SVATON, C. D. PLATT, S. HAMBLETON, O. NETH, G. GOSSE, S. REINSCH, D. HOLZINGER, Y. J. KIM, S. BAKHTIAR, F. ATSCHEKZEI, R. SCHMIDT, G. SOGKAS, S. CHANDRAKASAN, W. RAE, B. DERFALVI, H. V. MARQUART, A. OZEN, A. KIYKIM, E. KARAKOC-AYDINER, P. KRÁLÍČKOVÁ, G. DE BREE, D. KIRITSI, M. G. SEIDEL, R. KOBBE, J. DANTZER, L. ALSINA, T. ARMANGUE, V. LOUGARIS, P. AGYEMAN, S. NYSTRÖM, D. BUCHBINDER, P. D. ARKWRIGHT a B. GRIMBACHER. Therapeutic options for CTLA-4 insufficiency. Journal of Allergy and Clinical Immunology. New York: Mosby-Elseiver, 2022, roč. 149, č. 2, s. 736-746. ISSN 0091-6749. Dostupné z: https://dx.doi.org/10.1016/j.jaci.2021.04.039.
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Základní údaje
Originální název Therapeutic options for CTLA-4 insufficiency
Autoři EGG, D., I. C. RUMP, N. MITSUIKI, J. ROJAS-RESTREPO, M. E. MACCARI, C. SCHWAB, A. GABRYSCH, K. WARNATZ, S. GOLDACKER, V. PATIÑO, D. WOLFF, S. OKADA, S. HAYAKAWA, Y. SHIKAMA, K. KANDA, K. IMAI, M. SOTOMATSU, M. KUWASHIMA, T. KAMIYA, T. MORIO, K. MATSUMOTO, T. MORI, Y. YOSHIMOTO, I. DYBEDAL, M. KANARIOU, Z. Y. KUCUK, H. CHAPDELAINE, L. PETRUZELKOVA, H. M. LORENZ, K. E. SULLIVAN, J. HEIMALL, M. MOUTSCHEN, Jiří LITZMAN (203 Česká republika, domácí), M. RECHER, M. H. ALBERT, F. HAUCK, S. SENEVIRATNE, J. PACHLOPNIK SCHMID, A. KOLIOS, G. UNGLIK, C. KLEMANN, S. SNAPPER, L. GIULINO-ROTH, Michael SVATON (203 Česká republika), C. D. PLATT, S. HAMBLETON, O. NETH, G. GOSSE, S. REINSCH, D. HOLZINGER, Y. J. KIM, S. BAKHTIAR, F. ATSCHEKZEI, R. SCHMIDT, G. SOGKAS, S. CHANDRAKASAN, W. RAE, B. DERFALVI, H. V. MARQUART, A. OZEN, A. KIYKIM, E. KARAKOC-AYDINER, P. KRÁLÍČKOVÁ, G. DE BREE, D. KIRITSI, M. G. SEIDEL, R. KOBBE, J. DANTZER, L. ALSINA, T. ARMANGUE, V. LOUGARIS, P. AGYEMAN, S. NYSTRÖM, D. BUCHBINDER, P. D. ARKWRIGHT a B. GRIMBACHER (garant).
Vydání Journal of Allergy and Clinical Immunology, New York, Mosby-Elseiver, 2022, 0091-6749.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30102 Immunology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 14.200
Kód RIV RIV/00216224:14110/22:00125671
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/j.jaci.2021.04.039
UT WoS 000752623200031
Klíčová slova anglicky CTLA-4; HSCT; LRBA; abatacept; common variable immunodeficiency; diagnosis; primary immunodeficiency; rituximab; sirolimus; treatment
Štítky 14110114, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 14. 3. 2023 12:37.
Anotace
Background: Heterozygous germline mutations in cytotoxic T lymphocyte-associated antigen-4 (CTLA4) impair the immunomodulatory function of regulatory T cells. Affected individuals are prone to life-threatening autoimmune and lymphoproliferative complications. A number of therapeutic options are currently being used with variable effectiveness. Objective: Our aim was to characterize the responsiveness of patients with CTLA-4 insufficiency to specific therapies and provide recommendations for the diagnostic workup and therapy at an organ-specific level. Methods: Clinical features, laboratory findings, and response to treatment were reviewed retrospectively in an international cohort of 173 carriers of CTLA4 mutation. Patients were followed between 2014 and 2020 for a total of 2624 months from diagnosis. Clinical manifestations were grouped on the basis of organ-specific involvement. Medication use and response were recorded and evaluated. Results: Among the 173 CTLA4 mutation carriers, 123 (71%) had been treated for immune complications. Abatacept, rituximab, sirolimus, and corticosteroids ameliorated disease severity, especially in cases of cytopenias and lymphocytic organ infiltration of the gut, lungs, and central nervous system. Immunoglobulin replacement was effective in prevention of infection. Only 4 of 16 patients (25%) with cytopenia who underwent splenectomy had a sustained clinical response. Cure was achieved with stem cell transplantation in 13 of 18 patients (72%). As a result of the aforementioned methods, organ-specific treatment pathways were developed. Conclusion: Systemic immunosuppressants and abatacept may provide partial control but require ongoing administration. Allogeneic hematopoietic stem cell transplantation offers a possible cure for patients with CTLA-4 insufficiency.
VytisknoutZobrazeno: 21. 7. 2024 02:29