Інформація призначена тільки для фахівців сфери охорони здоров'я, осіб,
які мають вищу або середню спеціальну медичну освіту.

Підтвердіть, що Ви є фахівцем у сфері охорони здоров'я.

Мобильная версия

Регистрация Забыли пароль?

Журнал "Гастроэнтерология" Том 55, №4, 2021

Вернуться к номеру

Вивчення тканинного IgG4 у слизовій оболонці товстої кишки в пацієнтів iз запальними захворюваннями кишечника

Вивчення тканинного IgG4 у слизовій оболонці товстої кишки в пацієнтів iз запальними захворюваннями кишечника

Авторы: Yu.M. Stepanov, T.S. Tarasova, M.V. Stoikevych, Yu.A. Gaydar, N.S. Fedorova
State Institution “Institute of Gastroenterology of the National Academy of Medical Sciences of Ukraine”, Dnipro, Ukraine

Рубрики: Гастроэнтерология

Разделы: Клинические исследования

Версия для печати


Резюме

Актуальність. На сьогодні запальні захворювання кишечника (ЗЗК) є глобальною проблемою, поширеність якої зростає в усьому світі. Це значно підвищує економічне навантаження на систему охорони здоров’я. Останнім часом у багатьох дослідженнях вказують на важливу роль імуноглобуліну G4 (IgG4) у формуванні хронічного запалення при ЗЗК і можливість використання його як біомаркера запального процесу. Мета: удосконалити діагностику хронічних запальних захворювань кишечника на підставі вивчення стану IgG4-позитивних плазматичних клітин у слизовій оболонці товстої кишки в пацієнтів із виразковим колітом (ВК) та хворобою Крона (ХК). Матеріали та методи. Обстежено 34 осіб із ЗЗК: 25 із ВК та 9 із ХК, із них 20 жінок та 14 чоловіків середнім віком (38,8 ± 3,0) та (38,2 ± 3,7) року відповідно. Пацієнти розподілені на групи залежно від нозології та тяжкості перебігу захворювання. В усіх хворих виконане ендоскопічне дослідження товстої кишки з метою встановлення або уточнення діагнозу, отримані біопсійні зразки для гістологічного та імуногістохімічного аналізу. Результати. У 13 (38,3 %) з 34 обстежених пацієнтів виявлений позитивний результат на наявність тканинного IgG4 (≥ 10 клітин у полі зору). Серед осіб із ВК 48,0 % мають позитивний результат імуногістохімічного дослідження на тканинний IgG4, у пацієнтів iз ХК цей показник становить 11,1 %, що дає нам можливість стверджувати, що при ВК підвищення тканинного IgG4 зустрічається в 4,4 раза частіше. При середньому ступені тяжкості ВК позитивний тканинний IgG4 виявляють в 1,1 раза частіше, ніж при тяжкому перебігу. У хворих із легким ступенем тяжкості тканинний IgG4 не виявлявся. Висновки. При ВК IgG4-позитивні клітини в слизовій оболонці товстої кишки зустрічаються частіше, ніж при ХК, що дає можливість використовувати цей показник для диференційної діагностики виразкового коліту і хвороби Крона. Позитивний тканинний IgG4 зустрічається частіше при середньому ступені тяжкості, ніж при тяжкому.

Background. Inflammatory bowel disease (IBD) is a global problem today, with a growing prevalence in the world. It significantly increases the economic burden on the health care system. Recently, many studies indicate the important role of immunoglobulin G4 (IgG4) in the formation of chronic inflammation in IBD and the possibility of using it as a biomarker of the inflammatory process. The purpose was to improve the diagnosis of chronic inflammatory bowel diseases by studying the status of IgG4-positive plasma cells in the mucous membrane of the colon in patients with ulcerative colitis (UC) and Crohn’s disease (CD). Materials and methods. We have examined 34 patients with IBD, 25 with UC and 9 with CD, of them 20 women and 14 men, with an average age of (38.8 ± 3.0) and (38.2 ± 3.7) years, respectively. Patients were divided into groups depending on the noso­logy and severity of the disease. All patients underwent endoscopic examination of the colon to establish or clarify the diagnosis, and biopsy specimens were taken for histological and immunohistochemical examination. Results. In 13 (38.3 %) of 34 examined patients, a positive result for the presence of tissue IgG4 (≥ 10 cells in the field of view) was found. Among patients with UC, 48 % have a positive result of immunohistochemical examination of tissue IgG4, in people with CD, this figure is 11.1 %. This gives us reason to say that in UC, elevation of tissue IgG4 levels occurs 4.4 times more often. Positive tissue IgG4 in patients with moderate UC was found 1.1 times more often than in severe UC. Among patients with mildly active disease, tissue IgG4 was not detected. Conclusions. In UC, IgG4-positive cells in the mucous layer of the colon are more common than in CD, which makes it possible to use this indicator for the differential diagnosis of ulcerative colitis and Crohn’s disease. Positive tissue IgG4 is more common in moderate form than in severe one.


Ключевые слова

запальні захворювання кишечника; виразковий коліт; хвороба Крона; IgG4

inflammatory bowel diseases; ulcerative colitis; Crohn’s disease; IgG4

doi: http://dx.doi.org/10.22141/2308-2097.55.4.2021.247916

Introduction

Today, inflammatory bowel disease (IBD) has become a global problem with increasing prevalence on all continents. It is estimated that more than 1 million people in the United States and 2.5 million in Europe have IBD, which significantly increases health care expenses. The main factors that influence the financial component are the cost of hospitalization and surgery. At the same time, the cost of reduced quality of life is difficult to measure but this component invariably affects patients and their families [1–3].
The term IBD was introduced to denote two conditions: ulcerative colitis (UC) and Crohn’s disease (CD). These nosologies are divided into categories depending on the severity of the disease, the location of the lesion and the duration of the disease [4, 5]. Diagnosis of inflammatory bowel disease is usually based on clinical, endoscopic, radiological, histological examinations. This is a standard that remains unchanged, despite the new understanding of the immunological and genetic component of IBD [1, 6, 7].
Inflammatory bowel diseases are chronic disorders that occur as a result of the interaction between genetic and environmental factors [8]. In most patients, IBD is diagnosed at a young age. The accurate etiology of IBD is unknown, and therefore causal therapy for this disease is not yet available [9].
The importance of the role of humoral immunity in the formation of chronic inflammation in IBD has been overlooked for many years, and only in the last 5 years, there have been studies that indicate the importance of B-lymphocytes in the pathogenesis of inflammation. B-lymphocytes are finally differentiated into plasma cells, which are characterized by the production of various antibodies. These antibodies are actively involved in the regulation of humoral immunity and can cause allergic reactions and multiple autoimmune disorders [10, 11]. Excessive plasmacytic infiltration in the lamina propria is a classic pathological characteristic of IBD, which indicates the potential involvement of B-cells in the pathogenesis of this condition [12, 13].
The study of the role of humoral immunity in the pathogenesis of IBD and the possibility of using immunoglobulins as inflammatory biomarkers is one of the promising directions of diagnosis. And the use of tissue biomarkers for the differential diagnosis of UC and CD will help expand and deepen the research area for IBD [12, 14, 15].
The main indicator of the status of humoral immunity is the content of immunoglobulins (IgA, IgM, IgG) [12]. IgG4, which is the smallest of all IgG isotypes, usually was ignored because it was considered a non-inflammatory antibody. However, its role in various autoimmune disorders and even in the occurrence of cancer has been the subject of research in recent years, along with the detection and prevalence of IgG4-related diseases [5, 11, 16].
IgG4 is a heterogeneous antibody, which may be directly pathogenic, has a protective role, or may be a random marker of an aberrant inflammatory response. IgG4 antibodies have exceptional structural and functional characteristics, indicating anti-inflammatory and resistance-promoting effects [17, 18]. This emphasizes the need for researches in this area, which aims at improving the diagnosis, the ability to predict these diseases that will allow improving the quality of treatment and life of patients with IBD.
The purpose was to improve the diagnosis of chronic inflammatory bowel diseases based on the study of IgG4-positive plasma cells in the mucous membrane of the colon in patients with ulcerative colitis and Crohn’s disease.

Materials and methods

We have examined 34 patients with IBD. There were 25 individuals with UC and 9 with CD, including 20 women and 14 men, with an average age of (38.8 ± 3.0) and (38.2 ± 3.7) years, respectively. Patients were divided into groups depending on the nosology and severity of the disease determined by the Mayo score (Table 1). Among people with UC, mild form (3–5 points) has been detected in 3 patients (group I), moderate (6–10 points) — in 18 (group II), and severe (11–12 points) — in 4 (group III). In patients with CD (group IV), the severity was evaluated by the Crohn’s disease activity index developed by W.R. Best (Table 2).
Patients were enrolled in the study regardless of gender and age.
Endoscopic examinations of the colon were performed according to conventional methods using a Pentax EC-380LKp video colonoscope (Japan) to establish or clarify the diagnosis, analyzing changes in the state of the colon mucosa, taking biopsy specimens for histological and immunohistochemical examinations.
To determine the endoscopic activity of UC, the Mayo score was used: remission (degree 0), mildly active (degree 1), moderately active (degree 2), severely active (degree 3) [19, 20]. This classification is based on the presence of changes and on the severity of macroscopic signs characteristic of UC: fade (loss) of vascular pattern, bleedings and defects of mucous membrane of the colon. It is proved that there is a strong relationship between the clinical activity of UC and the severity of endoscopic signs, as well as the prevalence of the colon lesions [21–23].
Typical signs of Crohn’s disease during endoscopic examination were the presence and severity of aphthae, deep longitudinal ulcers, cobblestone appearance, pseudopolyposis, strictures, and changes in the perianal area.
Immunohistochemical studies of biopsy material were performed on deparaffinized sections of the intestine, 3–5 μm thick. On the prepared sections, we applied 50–100 μm of rabbit serum diluted 1 : 200 (Abcam, USA) at +5 °C in a wet chamber for 8 hours. After that sections were washed in phosphate-buffered saline, pH 7.4, three times for 5 minutes. Avidin-streptavidin complex labeled with horseradish peroxidase was applied for 60 minutes. Then horseradish peroxidase was visualized with 0.005% solution of 3,3-tetrahydrochloride benzidine (Sigma, USA) in phosphate-buffered saline, pH 7.4. The number of IgG4-positive plasma cells was counted in 5 consecutive fields of view. A case was considered positive when ≥ 10 IgG4-positive cells were detected in one field of view in sections.
To optimize the results and automate data processing, the obtained indicators were entered into the database management system, which is created using the integrated application package Statistica for Windows 6.0.
Descriptive and inductive statistics were used for statistical data analysis. The average values of variables were compared by means of parametric methods (Student’s t-test) with a normal distribution of these features expressed in the interval scale. The χ2 goodness of fit test was used to compare qualitative indicators. Differences between the two indicators were considered probable at p < 0.05 [24–26].

Results and discussions

Chronic relapsing course was observed in most patients with IBD. In 7 people, 5 with UC and 2 with CD, the diagnosis was established for the first time. The mean duration of IBD was (4.4 ± 0.7) years with no significant difference between groups.
As for the extent of intestinal lesions in patients of groups I and II, left-sided lesions of the colon are more typical (66.7 %). In group III, more extensive lesions of the colon were detected (50.0 % — left-sided and 50.0 % — total) (Fig. 1). In patients with CD (group IV), terminal ileitis prevailed (55.6 %).
The analysis revealed that in group I the remission stage prevailed (66.7 %) and a third of patients had a minimal stage of activity; in the group with moderate disease, the pronounced activity of ulcerative colitis prevailed in 55.6 % (p < 0.05) of cases, and in group III, all patients had severely active disease (p < 0.05).
In patients with Crohn’s disease, segmental lesions of the colon dominated (77.8 %), when foci of inflammation with defects alternate with areas of unchanged mucous layer. Left-sided colon lesions (44.4 %) were more frequent, in a third of patients, the terminal ileum was involved in the inflammatory process. Total colitis and rectal lesions were detected with a frequency of 11.1 %, in 2 cases (22.2 %), there was a lesion of the perianal area in the form of scarring, which indicated previous fistulas (Fig. 2).
In 55.5 % of patients, fibrotic strictures of the colon were determined, most of them were localized in the sigmoid section of the colon that is typical for CD. Two people (22.2 %) had fistulas.
To detect tissue IgG4, immunohistochemical staining of biopsy material was performed. The accumulation of IgG4-positive cells in UC and CD is shown in Fig. 3, 4.
In 13 (38.3 %) of 34 examined patients, a positive result for the presence of tissue IgG4 (≥ 10 cells in the field of view) was found. In 7 (20.5 %) people, the amount of IgG4 cells was 3–5 in the field of view, in 14 (41.2 %) cases, IgG4-positive cells were not detected (Fig. 5, 6).
In 48 % of patients with UC, the result of immunohistochemical examination for tissue IgG4 was positive. Among patients with CD, this figure was 11.1 % that allows us to say that in UC, tissue IgG4 elevation occurred 4.4 times more often.
Among 18 patients with moderate UC according to the Mayo score, a positive result for tissue IgG4 was found in 10 (55.5 %) cases, and in those with severely active disease — in 2 of 4 (50.0 %) (Fig. 7).
From the above data, we can conclude that with moderate severity of UC, positive tissue IgG4 is found 1.1 times more often than in severe UC. Among patients with mild severity, positive tissue IgG4 was not detected. Given the small sample of patients with CD, these data require further study.

Conclusions

1. More extensive lesions of the colon have been found in patients with severe UC than in those with mildly and moderately active disease.
2. In ulcerative colitis, IgG4-positive cells in the coloniс mucosa are found 4.4 times more often than in Crohn’s disease, which may allow using this indicator for the differential diagnosis of UC and CD.
3. There was a tendency to more frequent detection of positive tissue IgG4 in moderate IBD than in severe.
4. It is planned to further study the dependence of tissue IgG4 levels in patients with IBD on the duration of the disease and the localization of lesions in the mucous membrane of the colon, which will allow developing methods to predict the severity of inflammatory bowel diseases, and in the future will help optimize therapy and improve the quality of life of patients.
 
Received 28.10.2021
Revised 15.11.2021
Accepted 22.11.2021

Список литературы

  1. Kaplan G.G. The global burden of IBD: from 2015 to 2025. Nature Reviews Gastroenterology & Hepatology. 2015. 12(12). 720-727. doi: 10.1038/nrgastro.2015.150.
  2. Sub Lee H., Jae Lee K. Immunoglobulin G4-related immune responses to common food antigens in patients with ulcerative colitis and Crohn’s disease. Turkish Journal of Gastroenterology. 2019. 5(5). 408-414. doi: 10.5152/tjg.2019.18466.
  3. Ng S.C. et al. Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies. Lancet. 2018. 390. 2769-2778. doi: 10.1016/S0140-6736(17)32448-0.
  4. Lee S.H., Kwon J., Cho M.L. Immunological pathogenesis of inflammatory bowel disease. Intestinal Research. 2018. 16(1). 26. doi: 10.5217/ir.2018.16.1.26.
  5. Šimurina M. et al. Glycosylation of immunoglobulin G associa–tes with clinical features of inflammatory bowel diseases. Gastroenterology. 2018. 154(5). 1320-1333. doi: 10.1053/j.gastro.2018.01.002.
  6. British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults. Gut. 2019. 68(3). 1-106. doi: 10.1136/gutjnl-2019-318484.
  7. Dietary guidance for patients with inflammatory bowel disease from the International Organization for the Study of Inflammatory Bowel Disease. Clinical Gastroenterology and Hepatology. 2020. 18. 1381-1392. doi: 10.1016/j.cgh.2020.01.046.
  8. Limketkai B.N., Wolf A., Parian A.M. Nutritional interventions in the patient with inflammatory bowel disease. Gastroenterology Clinics of North America. 2018. 47(1). 155-177. doi: 10.1016/j.gtc.2017.09.007.
  9. Guan Q.A. Comprehensive review and update on the pathogenesis of inflammatory bowel disease. J. Immunol. Res. 2019 Dec 1. 2019. 7247238. doi: 10.1155/2019/7247238.
  10. Armstrong H. et al. Host immunoglobulin G selectively identifies pathobionts in pediatric inflammatory bowel disease. Microbiome. 2019. 7(1). 1-17. doi: 10.1186/s40168-018-0604-3.
  11. Wang Z. et al. High level of IgG4 as a biomarker for a new subset of inflammatory bowel disease. Scientific Reports. 2018. 8(1). 10018. doi: 10.1038/s41598-018-28397-8.
  12. European consensus on the histopathology of inflammatory bowel disease. Journal of Crohn’s and Colitis. 2013. 7(10). 827-851. doi: 10.1016/j.crohns.2013.06.001.
  13. Smids C. et al. The value of serum antibodies in differentiating inflammatory bowel disease, predicting disease activity and disease course in the newly diagnosed patient. Scandinavian Journal of Gastroenterology. 2017. 52(10). 1104-1112. doi: 10.1080/00365521.2017.1344875.
  14. Dmochowska N., Wardill H.R., Hughes P.A. Advances in imaging specific mediators of inflammatory bowel disease. International Journal of Molecular Sciences. 2018. 19(9). 2471. doi: 10.3390/ijms19092471.
  15. Šimurina M. et al. Glycosylation of immunoglobulin G associates with clinical features of inflammatory bowel diseases. Gastroenterology. 2018. 154(5). 1320-1333. doi: 10.1053/j.gastro.2018.01.002.
  16. Chen X. et al. IgG4+ plasma cell infiltration is correlated with the development of inflammatory bowel disease and can be regulated by TLR-4. Int. J. Clin. Exp. Pathol. 2018. 11(9). 4537-4544.
  17. Trampert D.C. et al. On the role of IgG4 in inflammatory conditions: lessons for IgG4-related disease. Biochimica et Biophysica Acta — Molecular Basis of Disease. 2018. 1864(4). 1401-1409. doi: 10.1016/j.bbadis.2017.07.038.
  18. Harkness T. et al. Immunoglobulin G and immunoglobulin G subclass concentrations differ according to sex and race. Annals of Allergy Asthma Immunology. 2020. 125. 190-195. doi: 10.1016/j.anai.2020.03.018.
  19. Lewis J.D., Chuai S., Nessel L., Lichtenstein G.R., Aberra F.N. Use of the noninvasive components of the Mayo score to assess clinical response in ulcerative colitis. Inflam. Bowel Dis. 2008. 14(12). 1660-1666. doi: 10.1002 ibd.20520.
  20. Lobatón T., Bessissow T., De Hertogh G., Lemmens B., Maedler C. The Modified Mayo Endoscopic Score (MMES): a new index for the assessment of extension and severity of endoscopic activity in ulcerative colitis patients. J. Crohn’s Colitis. 2015 Oct. 9(10). 846-52. doi: 10.1093/ecco-jcc/jjv111.
  21. Restellini S., Chao C.-Y., Martel M., Affif W. Clinical parameters correlate with endoscopic activity of ulcerative colitis: a systematic review. Clinical Gastroenterology and Hepatology. 2019. 17(7). 1265-1275.e8. doi: 10.1016/j.cgh.2018.12.021.
  22. Gionchetti P., Dignass A., Danese S., Magro F.J. Dias. 3rd European Evidence-based Consensus on the Diagnosis and Management of Crohn’s Disease 2016. Part 2: surgical management and special situations. Journal of Crohn’s and Colitis. 2017. 11(2). 135-149. doi: 10.1093/ecco-jcc/jjw169.
  23. Vashist M.N., Samaan M., Mosli M.H., Parker C.E. Endoscopic scoring indices for evaluation of disease activity in ulcerative colitis. Cochrane Database Syst. Rev. 2018 Jan 16. 1(1). CD011450. doi: 10.1002/14651858.CD011450.pub2.
  24. Петри А., Сэбин К. Наглядная статистика в медицине. Москва: Гэотар-Мед, 2003. 143 с.
  25. Иванова В.С. Основы математической статистики. Москва, 1990. 174 с.
  26. Енюков И.С. Методы, алгоритмы, программы многомерного статистического анализа. Москва: Финансы и статистика, 1986. 86 с.

Вернуться к номеру