Справка
x
Поиск
Закладки
Озвучить книгу
Изменить режим чтения
Изменить размер шрифта
Оглавление
Для озвучивания и цитирования книги перейдите в режим постраничного просмотра.
Первичные иммунодефициты с преимущественной недостаточностью синтеза антител
Список литературы
Поставить закладку
Gupta A. Primary Immunodeficiency Disorders: Where Do We Stand? // Indian J. Pediatr. 2019. Т. 86, № 10. С. 873–874.
Hartono S. и др. Gastrointestinal Disorders Associated with Primary Immunodeficiency Diseases // Clin. Rev. Allergy Immunol. 2019. Т. 57, № 2. С. 145–165.
Bonilla F.A. и др. Practice parameter for the diagnosis and management of primary immunodeficiency // J. Allergy Clin. Immunol. 2015. Т. 136, № 5. С. 1186–1205.
Rezaei N. и др. An Introduction to Primary Immunodeficiency Diseases // Primary Immunodeficiency Diseases. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. С. 1–38.
Tangye S.G. и др. Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee // J. Clin. Immunol. 2020.
Aghamohammadi A. и др. Predominantly Antibody Deficiencies // Primary Immunodeficiency Diseases. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. С. 183–244.
Fried A.J., Bonilla F.A. Pathogenesis, Diagnosis, and Management of Primary Antibody Deficiencies and Infections // Clin. Microbiol. Rev. 2009. Т. 22, № 3. С. 396–414.
Латышева Е.А. Первичные иммунодефициты у взрослых. Преимущественное нарушение синтеза антител // Терапия. 2018. № 7-8 (25-26). С. 119–124.
van der Burg M. и др. New frontiers of primary antibody deficiencies // Cell. Mol. Life Sci. 2012. Т. 69, № 1. С. 59–73.
Picard C. и др. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity // J. Clin. Immunol. 2018. Т. 38, № 1. С. 96–128.
Bogaert D.J.A. и др. Genes associated with common variable immunodeficiency: one diagnosis to rule them all? // J. Med. Genet. 2016. Т. 53, № 9. С. 575–590.
Bonilla F.A. и др. International Consensus Document (ICON): Common Variable Immunodeficiency Disorders // J. Allergy Clin. Immunol. Pract. 2016. Т. 4, № 1. С. 38–59.
Abbott J.K., Gelfand E.W. Common Variable Immunodeficiency // Immunol. Allergy Clin. North Am. 2015. Т. 35, № 4. С. 637–658.
Javier F.C., Moore C.M., Sorensen R.U. Distribution of primary immunodeficiency diseases diagnosed in a pediatric tertiary hospital // Ann. Allergy, Asthma Immunol. 2000. Т. 84, № 1. С. 25– 30.
Щербина А.Ю., Кузьменко Н.Б. Классификация первичных иммунодефицитов как отражение современных представлений об их патогенезе и терапевтических подходах. 2017. № 3. С. 51–57.
World Health Organization. International statistical classification of diseases and related health problems. - 10th revision, volume 1 tabilar list, Fifth edition, 2016. 2016. 242–244 с.
Bierry G. и др. Thoracic Manifestations of Primary Humoral Immunodeficiency: A Comprehensive Review // RadioGraphics. 2009. Т. 29, № 7. С. 1909–1920.
Hampson F.A. и др. Respiratory disease in common variable immunodeficiency and other primary immunodeficiency disorders // Clin. Radiol. 2012. Т. 67, № 6. С. 587–595.
Латышева Т.В. и др. Пульмунологические проявления у взрослых пациентов с дефектом гуморального звена иммунитета // Терапевтический архив. 2016. № 8. С. 127–134.
Suri D., Rawat A., Singh S. X-linked Agammaglobulinemia // Indian J. Pediatr. 2016. Т. 83, № 4. С. 331–337.
Abolhassani H. и др. A review on guidelines for management and treatment of common variable immunodeficiency // Expert Rev. Clin. Immunol. 2013. Т. 9, № 6. С. 561–575.
Chapel H. и др. Common variable immunodeficiency disorders: division into distinct clinical phenotypes // Blood. 2008. Т. 112, № 2. С. 277–286.
Popa V., Colby T. V., Reich S.B. Pulmonary Interstitial Disease in Ig Deficiency // Chest. 2002. Т. 122, № 5. С. 1594–1603.
Jesenak M. и др. Pulmonary Manifestations of Primary Immunodeficiency Disorders in Children // Front. Pediatr. 2014. Т. 2.
Verbsky J., Routes J. Sarcoidosis and Common Variable Immunodeficiency: Similarities and Differences // Semin. Respir. Crit. Care Med. 2014. Т. 35, № 03. С. 330–335.
Uzzan M. и др. Gastrointestinal Disorders Associated with Common Variable Immune Deficiency (CVID) and Chronic Granulomatous Disease (CGD) // Curr. Gastroenterol. Rep. 2016. Т. 18, № 4. С. 17.
Khokar A., Gupta S. Clinical and Immunological Features of 78 Adult Patients with Primary Selective IgG Subclass Deficiencies // Arch. Immunol. Ther. Exp. (Warsz). 2019. Т. 67, № 5. С. 325– 334.
ESID diagnostic criteria for PID [Электронный ресурс]. URL:
https://esid.org/layout/set/print/content/view/full/12919#Q7
.
Seidel M.G. и др. The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity // J. Allergy Clin. Immunol. Pract. 2019. Т. 7, № 6. С. 1763–1770.
ESID Registry – Working Definitions for Clinical Diagnosis of PID. 2019.
Patel S.Y., Carbone J., Jolles S. The Expanding Field of Secondary Antibody Deficiency: Causes, Diagnosis, and Management // Front. Immunol. 2019. Т. 10.
Chen X.-F. и др. Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia // Medicine (Baltimore). 2016. Т. 95, № 32. С. e4544.
Sanges S. и др. Diagnosis of primary antibody and complement deficiencies in young adults after a first invasive bacterial infection // Clin. Microbiol. Infect. 2017. Т. 23, № 8. С. 576.e1-576.e5.
Jolles S. The Variable in Common Variable Immunodeficiency: A Disease of Complex Phenotypes // J. Allergy Clin. Immunol. Pract. 2013. Т. 1, № 6. С. 545–556.
Gupta S., Pattanaik D., Krishnaswamy G. Common Variable Immune Deficiency and Associated Complications // Chest. 2019. Т. 156, № 3. С. 579–593.
McCullagh B.N. и др. Antibody deficiency in patients with frequent exacerbations of Chronic Obstructive Pulmonary Disease (COPD) // PLoS One / подред. Kostikas K. 2017. Т. 12, № 2. С. e0172437.
McCusker C., Upton J., Warrington R. Primary immunodeficiency // Allergy, Asthma Clin. Immunol. 2018. Т. 14, № S2. С. 61.
Orange J.S. и др. Use and interpretation of diagnostic vaccination in primary immunodeficiency: A working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology // J. Allergy Clin. Immunol. 2012. Т. 130, № 3. С. S1–S24.
Saha B.K. и др. Molecular and structural characterization of five novel mutations in the Bruton’s tyrosine kinase gene from patients with X-linked agammaglobulinemia. // Mol. Med. 1997. Т. 3, № 7. С. 477–485.
Yel L. и др. Mutations in the Mu Heavy-Chain Gene in Patients with Agammaglobulinemia // N. Engl. J. Med. 1996. Т. 335, № 20. С. 1486–1493.
Ferrari S. и др. Mutations of the Igβ gene cause agammaglobulinemia in man // J. Exp. Med. 2007. Т. 204, № 9. С. 2047–2051.
Minegishi Y. и др. Mutations in Igα (CD79a) result in a complete block in B-cell development // J. Clin. Invest. 1999. Т. 104, № 8. С. 1115–1121.
Minegishi Y. An Essential Role for BLNK in Human B Cell Development // Science (80-. ). 1999. Т. 286, № 5446. С. 1954–1957.
Minegishi Y. и др. Mutations in the Human λ5/14.1 Gene Result in B Cell Deficiency and Agammaglobulinemia // J. Exp. Med. 1998. Т. 187, № 1. С. 71–77.
Tang P. и др. Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1 // J. Clin. Immunol. 2018. Т. 38, № 1. С. 88–95.
Boisson B. и др. A recurrent dominant negative E47 mutation causes agammaglobulinemia and BCR– B cells // J. Clin. Invest. 2013. Т. 123, № 11. С. 4781–4785.
Stoddard J.L. и др. Targeted NGS: A Cost-Effective Approach to Molecular Diagnosis of PIDs // Front. Immunol. 2014. Т. 5.
Al-Mousa H. и др. Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases // J. Allergy Clin. Immunol. 2016. Т. 137, № 6. С. 1780–1787.
Cunningham-Rundles C. How I treat common variable immune deficiency // Blood. 2010. Т. 116, № 1. С. 7–15.
O’Keefe A. и др. Primary immunodeficiency for the primary care provider // Paediatr. Child Health. 2016. Т. 21, № 2. С. e10–e14.
Mohammadinejad P. и др. Antibiotic resistance in patients with primary immunodeficiency disorders versus immunocompetent patients // Expert Rev. Clin. Immunol. 2015. Т. 11, № 10. С. 1163–1172.
Feydy A. и др. Chest high resolution CT in adults with primary humoral immunodeficiency // Br. J. Radiol. 1996. Т. 69, № 828. С. 1108–1116.
Gharagozlou M. и др. Pulmonary complications in primary hypogammaglobulinemia: a survey by high resolution CT scan // Monaldi Arch. Chest Dis. 2016. Т. 65, № 2.
Malamut G. и др. The Enteropathy Associated With Common Variable Immunodeficiency: The Delineated Frontiers With Celiac Disease // Am. J. Gastroenterol. 2010. Т. 105, № 10. С. 2262–2275.
Eropean Medicines Agency. Guideline on the clinical investigation of human normal immunoglobulin for intravenous administration (IVIg) [Электронный ресурс]. 2018. URL:
https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-clinical-investigation-human-
normal-immunoglobulin-intravenous-administration-ivig-rev-3_en.pdf.
World Health Organization. World Health Organization Model List of Essential Medicines 21st List [Электронный ресурс]. 2019. URL:
https://www.who.int/medicines/publications/essentialmedicines/en/.
Ochs H.D., Pinciaro P.J. Octagam ® 5%, an Intravenous IgG Product, Is Efficacious and Well Tolerated in Subjects with Primary Immunodeficiency Diseases // J. Clin. Immunol. 2004. Т. 24, № 3. С. 309–314.
Stein M.R. и др. Safety and Efficacy of Privigen®, a Novel 10% Liquid Immunoglobulin Preparation for Intravenous Use, in Patients with Primary Immunodeficiencies // J. Clin. Immunol. 2009. Т. 29, № 1. С. 137–144.
Stein M.R. и др. Safety and efficacy of Home-Based Subcutaneous Immunoglobulin G in Elderly Patients with Primary Immunodeficiency Diseases // Postgrad. Med. 2011. Т. 123, № 5. С. 186–193.
Латышева Т.В., Латышева Е.А., Мартынова И.А. Место иммуноглобулинов для внутривенного введения в современной клинической практике: новый 10% иммуноглобулин. 2016. № 4. С. 82–87.
Хлудова Л.Г. и др. Оценка эффективности и безопасности 10% внутривенного иммуноглобулина привиджен в реальной клинической практике // Российский аллергологический журнал. 2019. № 4. С. 48–56.
Смирнова И.Н. и др. Фармакоэкономический анализ заместительной терапии внутривенным иммуноглобулином у пациентов с первичными дефектами гуморального звена иммунитета // Вопросы гематологии/онкологии и иммунопатологии в педиатрии. 2016. Т. 15, № 1. С. 66–71.
Radosevich M., Burnouf T. Intravenous immunoglobulin G: trends in production methods, quality control and quality assurance // Vox Sang. 2010. Т. 98, № 1. С. 12–28.
Laursen I.A. и др. Development, Manufacturing and Characterization of a Highly Purified, Liquid Immunoglobulin G Preparation from Human Plasma // Transfus. Med. Hemotherapy. 2014. Т. 41, № 3. С. 205–212.
Киргизов К.И., Скоробогатова Е.В. Внутривенные иммуноглобулины: применение современных физиологичных растворов способно улучшить результаты терапии // Российский журнал детской онкологии и гематологии. 2015. Т. 2, № 2. С. 77.
Wasserman R.L. Personalized Therapy: Immunoglobulin Replacement for Antibody Deficiency. // Immunol. Allergy Clin. North Am. 2019. Т. 39, № 1. С. 95–111.
Garcia-Lloret M., McGhee S., Chatila T.A. Immunoglobulin Replacement Therapy in Children // Immunol. Allergy Clin. North Am. 2008. Т. 28, № 4. С. 833–849.
Кондратенко И.В., Бологов А.А. Внутривенные иммуноглобулины от создания до наших дней. 2018. № 6. С. 124–132.
Латышева Т.В., Латышева Е.А., Мартынова И.А. Оценка эффективности и безопасности препарата иммуноглобулина для внутривенного введения И.Г.Вена у пациентов с первичным иммунодефицитом с преимущественным нарушением синтеза антитела // Российский аллергологический журнал. 2016. № 1. С. 16–22.
Eijkhout H.W. и др. The Effect of Two Different Dosages of Intravenous Immunoglobulin on the Incidence of Recurrent Infections in Patients with Primary Hypogammaglobulinemia // Ann. Intern. Med. 2001. Т. 135, № 3. С. 165.
Goudouris E.S. и др. II Brazilian Consensus on the use of human immunoglobulin in patients with primary immunodeficiencies // Einstein (São Paulo). 2017. Т. 15, № 1. С. 1–16.
Абрамова И.Н., Родина Ю.А., Щербина А.Ю. Эволюция препаратов внутривенных иммуноглобулинов и их клинического применения в педиатрической практике // Педиатрия Журнал им Г.Н. Сперанского. 2019. № 4. С. 210–217.
Walsh J.E. и др. Immunoglobulin replacement therapy reduces chronic rhinosinusitis in patients with antibody deficiency // Int. Forum Allergy Rhinol. 2017. Т. 7, № 1. С. 30–36.
Joud Hajjar и др. Prophylactic Antibiotics Versus Immunoglobulin Replacement in Specific Antibody Deficiency // J. Clin. Immunol. 2019.
Schwartz H.J. и др. The response to intravenous immunoglobulin replacement therapy in patients with asthma with specific antibody deficiency. // Allergy asthma Proc. Т. 27, № 1. С. 53–58.
Duse M. и др. Transient Hypogammaglobulinemia of Infancy: Intravenous Immunoglobulin as First Line Therapy // Int. J. Immunopathol. Pharmacol. 2010. Т. 23, № 1. С. 349–353.
Breslin M.E. и др. Transient hypogammaglobulinemia and severe atopic dermatitis: Open-label treatment with immunoglobulin in a case series // Allergy Rhinol. 2016. Т. 7, № 2. С. 69–73.
Abdou N.I. и др. Efficacy of Intravenous Gammaglobulin for Immunoglobulin G Subclass and/or Antibody Deficiency in Adults // Int. Arch. Allergy Immunol. 2009. Т. 149, № 3. С. 267–274.
Abrahamian F., Agrawal S., Gupta S. Immunological and clinical profile of adult patients with selective immunoglobulin subclass deficiency: response to intravenous immunoglobulin therapy // Clin. Exp. Immunol. 2010. Т. 159, № 3. С. 344–350.
Olinder-Nielsen A.-M. и др. Immunoglobulin prophylaxis in 350 adults with IgG subclass deficiency and recurrent respiratory tract infections: A long-term follow-up // Scand. J. Infect. Dis. 2007. Т. 39, № 1. С. 44–50.
Visitsunthorn N. и др. Immunoglobulin G (IgG) subclass deficiency in Thai children. // Asian Pacific J. allergy Immunol. 2011. Т. 29, № 4. С. 332–337.
Hanson L.A. и др. IgG subclass deficiency with or without IgA deficiency. // Clin. Immunol. Immunopathol. 1991. Т. 61, № 2 Pt 2. С. S70-7.
Quartier P. и др. Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: A retrospective survey of 31 patients // J. Pediatr. 1999. Т. 134, № 5. С. 589–596.
Gelfand E.W. Differences between IGIV products: Impact on clinical outcome // Int. Immunopharmacol. 2006. Т. 6, № 4. С. 592–599.
Camcoglu Y. Immunoglobulin Treatment of Immunodeficient Patients // Immunodeficiency. InTech, 2012.
Maarschalk-Ellerbroek L.J., Hoepelman I.M., Ellerbroek P.M. Immunoglobulin treatment in primary antibody deficiency // Int. J. Antimicrob. Agents. 2011. Т. 37, № 5. С. 396–404.
Латышева Е.А. и др. Персонифицированный подход – основа успеха при выборе препарата для заместительной терапии у пациентов с ПИД. // Российский аллергологический журнал. 2020. Т. 17, № 2. С. 81–101.
Brown K.E., Young N.S. Parvoviruses and Bone Marrow Failure // Stem Cells. 1996. Т. 14, № 2. С. 151–163.
Adams S.T.M. и др. Common Variable Immunodeficiency Presenting With Persistent Parvovirus B19 Infection // Pediatrics. 2012. Т. 130, № 6. С. e1711–e1715.
Ruiz Gutiérrez L. и др. Parvovirus B19 chronic monoarthritis in a patient with common variable immunodeficiency // Reumatol. Clínica. 2015. Т. 11, № 1. С. 58–59.
Sun A., Teschner W., Yel L. Improving patient tolerability in immunoglobulin treatment: focus on stabilizer effects // Expert Rev. Clin. Immunol. 2013. Т. 9, № 6. С. 577–587.
Chérin P., Cabane J. Relevant Criteria for Selecting an Intravenous Immunoglobulin Preparation for Clinical Use // BioDrugs. 2010. Т. 24, № 4. С. 211–223.
Dantal J. Intravenous Immunoglobulins: In-Depth Review of Excipients and Acute Kidney Injury Risk // Am. J. Nephrol. 2013. Т. 38, № 4. С. 275–284.
Shapiro R.S. Why I Use Subcutaneous Immunoglobulin (SCIG) // J. Clin. Immunol. 2013. Т. 33, № S2. С. 95–98.
Shabaninejad H. и др. A Comparative Study of Intravenous Immunoglobulin and Subcutaneous Immunoglobulin in Adult Patients with Primary Immunodeficiency Diseases: A Systematic Review and Meta-Analysis // Expert Rev. Clin. Immunol. 2016. Т. 12, № 5. С. 595–602.
Bonilla F.A. Intravenous and subcutaneous immunoglobulin G replacement therapy // Allergy Asthma Proc. 2016. Т. 37, № 6. С. 426–431.
N. Shah S., Todoric K., . Tarrant T.K. Improved outcomes on subcutaneous IgG in patients with humoral immunodeficiency and co-morbid bowel disease // Clin. Case Reports Rev. 2015. Т. 1, № 7.
Garbett N.D., Currie D.C., Cole P.J. Comparison of the clinical efficacy and safety of an intramuscular and an intravenous immunoglobulin preparation for replacement therapy in idiopathic adult onset panhypogammaglobulinaemia. // Clin. Exp. Immunol. 1989. Т. 76, № 1. С. 1–7.
García Rodríguez C. и др. [Treatment of primary immunodeficiencies with intravenous gamma globulin]. // An. Esp. Pediatr. 1987. Т. 27, № 6. С. 411–415.
Kuruvilla M., de la Morena M.T. Antibiotic Prophylaxis in Primary Immune Deficiency Disorders // J. Allergy Clin. Immunol. Pract. 2013. Т. 1, № 6. С. 573–582.
Kamae C. и др. Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles // J. Allergy Clin. Immunol. 2013. Т. 131, № 5. С. 1437-1440.e5.
Nakagawa N. и др. Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects // J. Allergy Clin. Immunol. 2011. Т. 128, № 1. С. 223-225.e2.
Korsunskiy I. и др. TREC and KREC Levels as a Predictors of Lymphocyte Subpopulations Measured by Flow Cytometry // Front. Physiol. 2019. Т. 9. С. 1877.
Rubin L.G. и др. 2013 IDSA Clinical Practice Guideline for Vaccination of the Immunocompromised Host // Clin. Infect. Dis. 2014. Т. 58, № 3. С. e44–e100.
Sobh A., Bonilla F.A. Vaccination in Primary Immunodeficiency Disorders // J. Allergy Clin. Immunol. Pract. 2016. Т. 4, № 6. С. 1066–1075.
Martire B. и др. Vaccination in immunocompromised host: Recommendations of Italian Primary Immunodeficiency Network Centers (IPINET) // Vaccine. 2018. Т. 36, № 24. С. 3541–3554.
Eibl M.M., Wolf H.M. Vaccination in patients with primary immune deficiency, secondary immune deficiency and autoimmunity with immune regulatory abnormalities // Immunotherapy. 2015. Т. 7, № 12. С. 1273–1292.
Латышева Т.В. и др. Вакцинация больных с первичными иммунодефицитами: современный взгляд на проблему // Российский аллергологический журнал. 2017. № 3. С. 19–26.
Хаитов Р.М., Сухих Г.Т. Ведение больных с Первичным иммунодефицитом в акушерстве. 2012.
Brinker K.A., Silk H.J. Common variable immune deficiency and treatment with intravenous immunoglobulin during pregnancy // Ann. Allergy, Asthma Immunol. 2012. Т. 108, № 6. С. 464–465.
Cunningham-Rundles C. Key aspects for successful immunoglobulin therapy of primary immunodeficiencies // Clin. Exp. Immunol. 2011. Т. 164. С. 16–19.
Gardulf A. и др. Rapid subcutaneous IgG replacement therapy at home for pregnant immunodeficient women. // J. Clin. Immunol. 2001. Т. 21, № 2. С. 150–154.
Palmeira P. и др. Transfer of antibodies across the placenta and in breast milk from mothers on intravenous immunoglobulin // Pediatr. Allergy Immunol. 2009. Т. 20, № 6. С. 528–535.
Özdemir Ö. Current Approach to Primary Immunodeficiency Diseases // South. Clin. Istanbul Eurasia. 2019.
Для продолжения работы требуется
Registration
Предыдущая страница
Следующая страница
Table of contents
Список сокращений
Термины и определения
Первичные иммунодефициты с преимущественной недостаточностью синтеза антител
+
Список литературы
Приложение А1. Состав рабочей группы по разработке и пересмотру клинических рекомендаций
Приложение А2. Методология разработки клинических рекомендаций
+
Приложение А3. Справочные материалы, включая соответствие показаний к применению и противопоказаний, способов применения и доз лекарственных препаратов, инструкции по применению лекарственного препарата
+
Приложение Б. Алгоритмы действий врача
+
Приложение В. Информация для пациента
Данный блок поддерживает скрол*