Abstract
Background
Inflammatory bowel disease (IBD) represents a series of digestive system abnormalities and parenteral manifestations. Stem cell therapy has been regarded as a promising treatment for IBD.
Methods
We searched Web of Science Core Collection for publications of interest from 1991 to 2019. Publication performance was analyzed using several bibliometric parameters, including Statplanet to reveal the geographic distribution of the publications, VOSviewer to identify the research landscape of hot topics, and CiteSpace to show keywords with the strongest citation bursts.
Results
A total of 1230 publications were identified, of which 674 articles were analyzed further. The United States was the most productive country and Spanish researchers published the highest quality articles. At a journal level, Gastroenterology published the greatest number of articles, while articles from Gut had the highest citation number. Results from the research landscape analysis of hot topics and the top 20 terms with the strongest citation bursts indicated that animal experiments, immunocytes, intestinal epithelial cells, cytokine expression, and clinical efficacy were the main focuses of research.
Conclusion
Stem cell therapy for IBD is currently receiving increasing attention by researchers, with focuses on animal experiments, immunocytes, intestinal epithelial cells, cytokine expression, and clinical efficacy.
Keywords: Stem cell therapy, inflammatory bowel disease, Crohn’s disease, ulcerative colitis, bibliometric analysis, animal experiment, immunocyte, intestinal epithelial cell, cytokine expression, clinical efficacy
Introduction
The spectrum of inflammatory bowel disease (IBD) is largely represented by Crohn’s disease (CD) and ulcerative colitis (UC). The diagnosis of IBD describes a chronic inflammatory gastrointestinal condition, potentially leading to a series of digestive system abnormalities and parenteral manifestations. IBDs were initially presumed to result from a dysregulated immune response to the intestinal microflora, influenced by environmental factors and genetic susceptibility.1–3 IBD has become a worldwide concern, with a prevalence surpassing 0.3% among western populations.4 Despite focused research, IBD remains a challenge for clinicians, with many yet undefined etiologic, pathogenic, and treatment-related factors.2 Traditional treatment modalities for IBD include 5-aminosalicylate, corticosteroids, and immunosuppressant drugs.5 The therapeutic effects of stem cell transplantation, as a promising therapy for various diseases, have also been studied intensively in relation to IBD. The properties underlying the therapeutic actions of stem cells include their unique self-renewal capacity, which enables their unlimited proliferation and differentiation.6 Mesenchymal stem cells (MSCs), also known as mesenchymal stromal cells, are multipotent stem cells that possess both infinite regeneration capacity and also immunosuppressive properties.7–9 Recent meta-analysis studies indicated both encouraging results and substantial challenges for MSC therapy in IBD,10,11 and stem cell therapy is likely to remain a research hotspot for years to come.
Knowledge of the current research landscape is necessary to understand progress in this field of research and to guide future studies. Bibliometrics was developed to allow the quantitative analysis of publications and citations. Bibliometric studies can describe research trends, present publication performances, and predict future research hotspots for a topic, thus helping researchers to understand important past research and to determine valuable future research directions. Increasing numbers of bibliometric studies are being published in various medical fields, including in relation to pneumonia, cardiovascular diseases, infectious diseases, and surgery.
As a long-term research hotspot and a potentially curative treatment for many difficult diseases, stem cell research has been the subject of bibliometric studies. However, to the best of our knowledge, there is currently no bibliometric analysis of stem cell therapy for IBD. The current study thus aimed to fill this gap by analyzing the bibliometric profile of stem cell therapy for the treatment of IBD, covering the years from 1991 to 2019. In this study, we present the bibliometric findings covering publication and citation trends for the past 19 years, as well as the publication performances of different countries, the top cited publications, and the overall focus trends.
Methods
The Web of Science Core Collection (WoSCC) comprises several databases that should not be used together for document retrieval.12,13 We searched the Science Citation Index Expanded and Conference Proceedings Citation Index-Science using the following search strategy to identify publications from 1991–2019, on “topic” including title, abstract, author’s keywords and KeyWords Plus®: (“stem cell” OR “stem cells” OR “progenitor cell” OR “progenitor cells” OR “stromal cell” OR “stromal cells”) AND ((“Crohn’s” OR “Crohn”) OR (“ulcerative colitis” OR “idiopathic proctocolitis” OR “colitis gravis”) OR (“inflammatory bowel”)). This resulted in the identification of 1986 publications. The full record and annual citation number of each document were download into Microsoft Excel 2016.
KeyWords Plus® provides algorithm-generated key words that appear in the references but not necessarily in the article. Terms in KeyWords Plus® could be irrelevant to the topic of a publication, and it is therefore inappropriate to use the above number of publications for analysis. Fu and Ho14 first proposed using only the title, abstract, and author key words to filter out documents of interest. In this study, 1230 of the 1986 identified documents were included as relevant to stem cell therapy for IBD.
This study analyzed the bibliometric information for number of publications in any single year, document type, journal, and publication geography.
In the WoSCC database, the corresponding author is named as the reprint author, and we therefore designated the first person in the author list as the corresponding author. The first author was considered as the first person in the author list. For single-author publications, the author was regarded as both the first and corresponding author. For publications in which the first person in the author list was also the corresponding author, this author was considered as both the first and corresponding author.
To analyze the bibliometric geography, it was necessary to know the home country for each study. We introduced several parameters, including TP (number of articles with at least one author from a certain country), IP (number of articles with authors from a single country), CP (number of articles with authors from multiple countries), FP (number of articles with first authors from a certain country), and RP (number of articles with corresponding author from a certain country). Articles published by Taiwanese authors were included under the country category “China”, and articles from Scotland, Wales, and Northern Ireland were reclassified under the country category “United Kingdom”. Notably, publications with multiple corresponding authors from different institutions were presumed to be collaborative studies from multiple centers, so all institutions were counted. We analyzed the countries in which these institutions were located and summarized the results in a color-coded map, generated using Statplanet (Statsilk, Sydney, Australia), to present a comprehensive view of the geographic distribution of publications of interest from 1991 to 2019.
We analyzed the citation life of the documents using five citation indicators, as used in previous studies:15,16 C0, number of times each publication was cited in the publication year; C2019, number of times each publication was cited in 2019; TC2019, number of times each publication was cited since its publication to 2019; TP, sum of a group of publications; and, CPP2019, being TC2019/TP.
We also used VOSviewer (www.vosviewer.com) to visualize the research network based on the abstract and title of each of the topic-related articles published in the most recent 10 years. The threshold was set to include words that occurred at least 20 times. We displayed all 168 items, which were automatically divided into four clusters by the built in algorithm. CiteSpace (http://cluster.cis.drexel.edu/∼cchen/citespace/) was then used to identify research trends by analyzing the top 20 terms with the strongest citation bursts from 1991 to 2019. Citation bursts indicated a sudden and increasingly rapid rise in citation counts, with the start and end of the citation surge marked by a red ring on the resultant image.
Results
Number of publications and citations per publication by year
Figure 1 shows the number of publications and citations per publication in each year from 1991 to 2019. The annual number of publications followed a general upward trend. Annual publications exceeded 150 for the first time in 2019. Interestingly, citations per publication continued to rise as publication numbers increased dramatically since 2009, indicating that this field has attracted increasing attention in recent years.
Document type of publications related to stem cell therapy for IBD
Publications related to stem cell therapy for IBD included six document types: 674 articles, 239 reviews, 31 editorial materials, 19 letters, 239 meeting abstracts, and three news items (Table 1). Articles and reviews were the predominant publication types, with CPP2019 values of 34.4 and 44.6, respectively. Reviews provided comprehensive summaries of what was known and were often cited more frequently than articles. However, articles were more significant in presenting research findings. In this study, the 674 identified articles were selected for further analysis.
Table 1.
Document type | TP2019 | % | TC2019 | CPP2019 |
---|---|---|---|---|
Article | 674 | 54.8% | 23217 | 34.4 |
Review | 264 | 21.5% | 11762 | 44.6 |
Editorial material | 31 | 2.5% | 111 | 3.6 |
Letter | 19 | 1.5% | 166 | 8.7 |
Meeting abstract | 239 | 19.4% | 62 | 0.3 |
News item | 3 | 0.2% | 0 | 0.0 |
TP: sum of group of publications; TC2019: number of times each publication cited since its publication to 2019; CPP2019: ratio of TC2019 to TP.
Top 10 most productive journals
The top 10 most productive journals are summarized in Table 2. Articles on this topic were published in 292 journals. Gastroenterology published the greatest number of articles (n = 27, 4.0%), followed by Inflammatory Bowel Diseases (n = 21, 3.1%). Articles published in Gut had the highest quality, and were cited an average of 110.1 times.
Table 2.
Journal | IF2019 | TP2019 | % | TC2019 | CPP2019 |
---|---|---|---|---|---|
Gastroenterology | 19.809 | 27 | 4.0 | 1940 | 71.9 |
Inflammatory Bowel Diseases | 4.005 | 21 | 3.1 | 320 | 15.2 |
Gut | 17.943 | 18 | 2.7 | 1981 | 110.1 |
Stem Cell Research & Therapy | 4.627 | 16 | 2.4 | 266 | 16.6 |
World Journal of Gastroenterology | 3.411 | 15 | 2.2 | 410 | 27.3 |
Cytotherapy | 4.297 | 11 | 1.6 | 223 | 20.3 |
Frontiers in Immunology | 4.716 | 11 | 1.6 | 56 | 5.1 |
Journal of Crohns & Colitis | 7.827 | 11 | 1.6 | 111 | 10.1 |
Plos One | 2.776 | 11 | 1.6 | 173 | 15.7 |
Terapevticheskii Arkhiv | 0.359 | 11 | 1.6 | 19 | 1.7 |
IF2019: impact factor in 2019; TP: sum of a group of publications; TC2019: number of times each publication cited since its publication to 2019; CPP2019: ratio of TC2019 to TP.
Global publication landscape
A color-coded map presenting a comprehensive view of the geographic distributions of the publications from 1991 to 2019 is shown in Figure 2. The detailed publication performances of the top 15 countries are shown in Table 3. A total of 46 countries have published articles related to stem cell therapy for IBD. The United States was the most productive country, accounting for more than 30% of the total number of articles, with the People’s Republic of China ranked second. Other countries that published more than 30 articles included the United Kingdom, Japan, Germany, Spain, and Italy. Spain and the Netherlands produced the most high quality research articles, with each article from these countries being cited on average 70.7 and 61.3 times, respectively.
Table 3.
Rank | Country | TP (%) | IP (R) | CP (R) | FP (R) | RP (R) | CPP2019 |
---|---|---|---|---|---|---|---|
1 | USA | 207 (30.7%) | 134 (1) | 73 (1) | 159 (1) | 165 (1) | 53.7 |
2 | China | 104 (15.4%) | 82 (2) | 22 (5) | 98 (2) | 97 (2) | 12.2 |
3 | United Kingdom | 75 (11.1%) | 32 (5) | 43 (2) | 51 (4) | 53 (4) | 44.5 |
4 | Japan | 72 (10.7%) | 57 (3) | 15 (9) | 60 (3) | 60 (3) | 20.3 |
5 | Germany | 64 (9.5%) | 32 (5) | 32 (3) | 42 (6) | 40 (6) | 50.6 |
6 | Spain | 52 (7.7%) | 38 (4) | 14 (10) | 48 (5) | 47 (5) | 70.7 |
Italy | 52 (7.7%) | 26 (7) | 26 (4) | 39 (7) | 39 (7) | 39.2 | |
8 | South Korea | 29 (4.3%) | 24 (8) | 5 (14) | 29 (8) | 29 (8) | 20.0 |
9 | Netherlands | 28 (4.2%) | 12 (9) | 16 (8) | 20 (9) | 21 (9) | 61.3 |
France | 28 (4.2%) | 8 (13) | 20 (6) | 15 (10) | 14 (10) | 35.9 | |
Canada | 28 (4.2%) | 9 (11) | 19 (7) | 13 (11) | 14 (10) | 28.0 | |
12 | Australia | 15 (2.2%) | 9 (11) | 6 (13) | 9 (13) | 9 (13) | 26.3 |
13 | Switzerland | 14 (2.1%) | 2 (15) | 12 (11) | 5 (15) | 5 (15) | 32.1 |
14 | Belgium | 13 (1.9%) | 5 (14) | 8 (12) | 6 (14) | 6 (14) | 42.5 |
Russia | 13 (1.9%) | 12 (9) | 1 (15) | 12 (12) | 12 (12) | 5.4 |
TP: sum of group of publications; IP: independent publication; CP: collaborative publication; FP: first-author publication; RP: reprint-author publication; R: rank; TC2019: number of times each publication cited since its publication to 2019; CPP2019: ratio of TC2019 to TP.
Top 10 most highly cited articles from 1991 and in 2019
The 10 most cited articles from 1991 to 2019 are shown in Table 4. The most cited article was published by Kontoyiannis et al.17 and reported on the defective function of tumor necrosis factor AU-rich elements in the development of IBD. Its citations accumulated quickly in the first few years after its publication, but manifested an overall downward trend from 2010 onwards. Interestingly, only three articles, including the most cited one, were published before the 21st century, and citations of these articles gradually declined. Information from classic papers was thus absorbed into the body of current knowledge, resulting in a decline in the annual number of citations.
Table 4.
Rank | First author | Journal title | Year | Article title | TC2019 |
---|---|---|---|---|---|
1 | Kontoyiannis, D.17 | Immunity | 1999 | Impaired on/off regulation of TNF biosynthesis in mice lacking TNF AU-rich elements: Implications for joint and gut-associated immunopathologies | 921 |
2 | Buonocore, S.51 | Nature | 2010 | Innate lymphoid cells drive interleukin-23-dependent innate intestinal pathology | 674 |
3 | Hermiston, M. L.52 | Science | 1995 | Inflammatory bowel-disease and adenomas in mice expressing a dominant-negative n-cadherin | 538 |
4 | Garcia-Olmo, D.53 | Diseases of the Colon & Rectum | 2005 | A phase I clinical trial of the treatment of Crohn’s fistula by adipose mesenchymal stem cell transplantation | 479 |
5 | Mombaerts, P.54 | Cell | 1993 | Spontaneous development of inflammatory bowel-disease in t-cell receptor mutant mice | 447 |
6 | Garcia-Olmo, D.55 | Diseases of the Colon & Rectum | 2009 | Expanded adipose-derived stem cells for the treatment of complex perianal fistula: a phase II clinical trial | 444 |
7 | Worthey, E. A.56 | Genetics in Medicine | 2011 | Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease | 433 |
8 | Allen, I. C.57 | Journal of Experimental Medicine | 2010 | The NLRP3 inflammasome functions as a negative regulator of tumorigenesis during colitis-associated cancer | 418 |
9 | Gonzalez-Rey, E.33 | Gut | 2009 | Human adult stem cells derived from adipose tissue protect against experimental colitis and sepsis | 394 |
10 | Duijvestein, M.58 | Gut | 2010 | Autologous bone marrow-derived mesenchymal stromal cell treatment for refractory luminal Crohn’s disease: results of a phase I study | 393 |
TC2019: number of times each publication was cited since its publication to 2019.
The 10 most cited articles in 2019 are shown in Table 5. None of these articles was published before 2009 and the most recent was published in 2017. The most cited article was published by Panés et al.18 and reported on the safety and efficacy of allogeneic adipose-derived stem cells (Cx601) for the treatment of refractory complex perianal fistulas. Although this article has had a short citation life, its citations increased dramatically, suggesting that it represents a growing momentum in this field.
Table 5.
Rank | First author | Journal title | Year | Article title | C2019 |
---|---|---|---|---|---|
1 | Panés, J.18 | Lancet | 2016 | Expanded allogeneic adipose-derived mesenchymal stem cells (Cx601) for complex perianal fistulas in Crohn’s disease: a phase 3 randomised, double-blind controlled trial | 104 |
2 | Buonocore, S.51 | Nature | 2010 | Innate lymphoid cells drive interleukin-23-dependent innate intestinal pathology | 70 |
3 | West, N. R.59 | Nature Medicine | 2017 | Oncostatin M drives intestinal inflammation and predicts response to tumor necrosis factor-neutralizing therapy in patients with inflammatory bowel disease | 61 |
4 | Onengut-Gumuscu, S.60 | Nature Genetics | 2015 | Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers | 47 |
5 | Garcia-Olmo, D.55 | Diseases of the Colon & Rectum | 2009 | Expanded Adipose-Derived Stem Cells for the Treatment of Complex Perianal Fistula: a Phase II Clinical Trial | 45 |
6 | Allen, I. C.57 | Journal of Experimental Medicine | 2010 | The NLRP3 inflammasome functions as a negative regulator of tumorigenesis during colitis-associated cancer | 43 |
7 | Gonzalez-Rey, E.33 | Gut | 2009 | Human adult stem cells derived from adipose tissue protect against experimental colitis and sepsis | 43 |
8 | Panés, J.61 | Gastroenterology | 2018 | Long-term efficacy and safety of stem cell therapy (Cx601) for complex perianal fistulas in patients with Crohn's disease | 41 |
9 | Gonzalez, M. A.62 | Gastroenterology | 2009 | Adipose-derived mesenchymal stem cells alleviate experimental colitis by inhibiting inflammatory and autoimmune responses | 39 |
10 | Ciccocioppo, R.63 | Gut | 2011 | Autologous bone marrow-derived mesenchymal stromal cells in the treatment of fistulising Crohn’s disease | 39 |
C2019: number of times each publication was cited in 2019.
Visualized landscape of research hotspots and top 20 terms with strongest citation bursts
The topic-related research hotspots, categorized into four groups, are shown in Figure 3. The green group mainly comprises research hotspots involving animal experiments and the construction of animal models; the red group represents research hotspots on cell and inflammatory cytokine expression; the yellow group mainly consists of research hotspots on treatment and clinical efficacy; and the blue group includes research hotspots on patient characteristics. The top 20 terms with the strongest citation bursts are listed in Table 6. The results basically confirmed previously detected research hotspots. “Mouse model” and “DSS-induced colitis” are related to animal models; “cell type” and “goblet cells” are related to cells; “tumor necrosis factor”, “Toll-like receptor”, and “pro-inflammatory cytokines” are related to cytokines; and “therapeutic effects”, “immunomodulatory property”, and “mucosal healing” are related to clinical efficacy.
Table 6.
Discussion
IBD is usually diagnosed at an early age and can substantially reduce patient quality of life. Although the incidence rate of IBD seems to have stabilized or even decreased in western countries since 1990, its prevalence has continued to increase worldwide, exceeding 0.3% in many developed countries.4 According to a report by Kaplan in 2015, more than 1 million people in the Americas and 2.5 million people in Europe were living with IBD.19 The lack of epidemiologic IBD data from developing nations suggests that the situation could be even worse, given an increase in incidence associated with recent industrialization.20,21
General information
The burden of IBD has urged clinicians to investigate new treatment modalities, including stem cell therapy. This novel and promising treatment has received increasing attention in recent decades, with only one publication per year for the first 3 years since 1991, annual publication numbers reaching double digits in 2002, and over 150 publications in 2019. CPPyear often drops with increasing publication numbers;15,22 however, the current study found that citations per publication continued to rise in the past decade, indicating that stem cell therapy for IBD is receiving increasingly more attention.
Geographical publication performances
In terms of publication performances of individual countries and institutions, the 15 most productive countries included nine in Europe (United Kingdom, Germany, Spain, Italy, The Netherlands, France, Switzerland, Belgium, Russia), three in Asia (China, Japan, South Korea), and two in North America (United States, Canada), along with Australia. IBD is estimated to have a high prevalence in developed countries and stem cell therapy remains a developing technique; it is therefore not surprising that the list is dominated by developed countries. American authors had the highest number of publications on stem cell research for IBD (n = 208, 30.9%), which was more than for the second and third countries combined. This was also shown to be the case in other medical fields, including stem cells in general, dengue, gynecology, and obstetrics.15,23,24 The United States also dominated in terms of first-author publications and reprint-author publications. Articles published by Spanish authors had the highest CPP2019 (70.7), followed by the Netherlands and the United States. Despite a large number of articles from China, they ranked last but one in terms of CPP2019, suggesting that Chinese authors need to publish more high quality studies. In addition to publication numbers and citations, we also calculated the number of international collaborative articles, given the increasing importance of international cooperation in today’s research. The United States participated in the most international collaborative studies, followed by Germany.
Research hotspots
Analysis of research hotspots and citation bursts identified animal models, biological behavior of cells, cytokine expression, and the clinical efficacy of stem cell therapy as research hotspots.
Animal experiments have been used increasingly to evaluate the efficacy and safety of MSC-based treatments.25 Although most preclinical in vivo data obtained from animal models have demonstrated the consistent efficacy of MSCs, clinical trials have provided conflicting results. This may be because the etiology and progression of human IBD are multifactorial, resulting in difficulties in building a suitable and reproducible animal model to symptomatically and morphologically reflect human IBD.26 In addition, immune differences between MSCs from humans and mice limit the translation of results from murine models to clinical situations.27,28 Ethical issues also influence the clinical application of novel treatment modalities such as stem cell therapy. Its potential benefits and risks have been discussed in relation to IBD, and it has been suggested that IBD patients should not typically receive stem cell therapy because IBD does not significantly reduce life expectancy and because multiple alternative effective treatments are available.29 Furthermore, whether stem cell therapy can achieve similar efficacy in IBD patients as in animal models is still controversial, and extreme care should thus be exercised in selecting patients for treatment and clinical trials. More efforts involving animal experiments are required to improve our understanding of the efficacy, safety, and mechanism of stem cell therapy, to allow it to be applied in suitable patients, with the expectation of a good prognosis.
The biological behavior of cells was also identified as a research hotspot, with immunocytes and intestinal epithelial cells being intensively studied.
Several investigators have reported that MSCs can inhibit cytokine secretion and the proliferation of T cells, B cells, natural killer cells, and dendritic cells in vitro.30–32 Gonzalez-Rey et al.33 confirmed that this inhibition was partially dependent on cell-to-cell contact between MSCs and peripheral blood mononuclear cells, resulting in reduced secretion of inflammatory cytokines and increased production of the cytokine IL-10. Another study showed that commonly used medications for IBD did not affect the functional capabilities of MSCs.34 The regenerative properties and immunoregulatory capacity of MSCs make them an attractive treatment option for use with standard CD therapy.
It is important to understand the role of intestinal epithelial cells in the pathogenesis of IBD, and how stem cell therapy can alter their function. There is widespread agreement that disruption of normal intestinal barrier function is particularly relevant to the development of IBD.35 This disruption impairs the defensive barrier maintained by rapidly proliferating epithelial cells thus making the intestine more susceptible to pathogens and other alimentary factors. Paneth cells, for example, are indispensable protective intestinal cells that produce antimicrobials, including the human α-defensins HD5 and HD6,36 and a decrease in the production of α-defensins by Paneth cells weakened the antimicrobial defenses of the ileal mucosa and was associated with IBD, especially ileal CD.36,37 Other evidence also showed inadequate expression of defensins in colonic CD.38 The mucus layer can protect the host from microbes in the lumen, and was found to be thinner, more variable, and partly denuded in patients with UC.39,40 Transplantation of intestinal epithelial stem cells is usually achieved by mucosal biopsies or by differentiation of autologous pluripotent stem cells,35,41 which are expected to differentiate into all types of intestinal epithelial cells to heal the damaged mucosa. In vitro studies confirmed that intestinal epithelial stem cells may constitute complementary treatment options for patients with mucosal damage.42,43
Cytokine expression has also drawn much attention. Abnormal cytokine expression levels may be related to genetic variations. Recent methodological advances in genetic analysis have greatly expanded our understanding of the genetic background of IBD,44 with the identification of more than 240 genetic risk loci for IBD. For example, NOD2, ATG16L1, and IRGM, which encode innate immunity proteins, play important roles in the development of IBD.45,46 CDH1 encodes E-cadherin, which facilitates cell adherent junctions, while PTPN22 encodes protein tyrosine phosphatase, nonreceptor type 22, which is important for intestinal barrier integrity.47 The risk gene IL23R could activate the transcription of proinflammatory cytokines and promote the differentiation of proinflammatory Th17 cells.48 However, animal models have shown that microbial colonization is a prerequisite, even under conditions of high permeability and genetic domination.49 Stem cell therapy heals the damaged intestinal barrier caused by a combination of genetic and external risk factors.
Limitations
This study had some limitations. First, the bibliometric information was only retrieved from WoSCC. Although Web of Science is believed to contain only important and influential journals because of its strict screening mechanism,50 a few papers on this topic may have been published in journals not included in Web of Science. Second, number of citations does not fully reflect the quality of a publication; for example, number of views could also be a good indicator of the influence of a publication, given that papers with a high number of views are important in educational settings.16
Conclusion
To the best of our knowledge, this study provides the first bibliometric analysis of publications on stem cell therapy for IBD. The past 10 years have witnessed a surge in research in this field, with most research articles published by authors in developed Western and developing East Asian countries. The United States was the most productive country, but articles by Spanish researchers had the highest average citation numbers. Further analysis showed that research attention was mainly focused on animal experiments, immunocytes, intestinal epithelial cells, cytokine expression, and clinical efficacy.
Acknowledgement
The author would like to thank Professor Yuh-Shan Ho for supporting this work.
Footnotes
Declaration of conflicting interest: The authors declare that there is no conflict of interest.
Funding: This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
ORCID iD: Yuming Chong https://orcid.org/0000-0001-9307-3046
References
- 1.Eichele DD, Young R. Medical management of inflammatory bowel disease. Surg Clin North Am 2019; 99: 1223–1235. DOI: 10.1016/j.suc.2019.08.011. [DOI] [PubMed] [Google Scholar]
- 2.Fiocchi C. Inflammatory bowel disease: etiology and pathogenesis. Gastroenterology 1998; 115: 182–205. [DOI] [PubMed] [Google Scholar]
- 3.Dave M, Papadakis KA, Faubion WA., Jr. Immunology of inflammatory bowel disease and molecular targets for biologics. Gastroenterol Clin North Am 2014; 43: 405–424. DOI: 10.1016/j.gtc.2014.05.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Ng SC, Shi HY, Hamidi N, et al. Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies. Lancet 2017; 390: 2769–2778. DOI: 10.1016/s0140-6736(17)32448-0. [DOI] [PubMed] [Google Scholar]
- 5.Su HJ, Chiu YT, Chiu CT, et al. Inflammatory bowel disease and its treatment in 2018: Global and Taiwanese status updates. J Formos Med Assoc 2019; 118: 1083–1092. DOI: 10.1016/j.jfma.2018.07.005. [DOI] [PubMed] [Google Scholar]
- 6.Müller FJ, Laurent LC, Kostka D, et al. Regulatory networks define phenotypic classes of human stem cell lines. Nature 2008; 455: 401–405. DOI: 10.1038/nature07213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Beyth S, Borovsky Z, Mevorach D, et al. Human mesenchymal stem cells alter antigen-presenting cell maturation and induce T-cell unresponsiveness. Blood 2005; 105: 2214–2219. DOI: 10.1182/blood-2004-07-2921. [DOI] [PubMed] [Google Scholar]
- 8.Campioni D, Bortolotti D, Baricordi OR, et al. Multipotent stromal cells skew monocytes towards an anti-inflammatory function: a role for HLA-G molecules. Haematologica 2013; 98: e114. DOI: 10.3324/haematol.2013.090092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Melief SM, Schrama E, Brugman MH, et al. Multipotent stromal cells induce human regulatory T cells through a novel pathway involving skewing of monocytes toward anti-inflammatory macrophages. Stem Cells 2013; 31: 1980–1991. DOI: 10.1002/stem.1432. [DOI] [PubMed] [Google Scholar]
- 10.Cheng F, Huang Z, Li Z. Mesenchymal stem-cell therapy for perianal fistulas in Crohn's disease: a systematic review and meta-analysis. Tech Coloproctol 2019; 23: 613–623. DOI: 10.1007/s10151-019-02024-8. [DOI] [PubMed] [Google Scholar]
- 11.Dave M, Mehta K, Luther J, et al. Mesenchymal stem cell therapy for inflammatory bowel disease: a systematic review and meta-analysis. Inflamm Bowel Dis 2015; 21: 2696–2707. DOI: 10.1097/MIB.0000000000000543. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Ho YS. Critical comment on: Zhu, Jin, and He ‘On evolutionary economic geography: a literature review using bibliometric analysis’. Eur Plan Stud 2019; 27: 1235–1237. [Google Scholar]
- 13.Ho YS. Rebuttal to: Su et al. “The neurotoxicity of nanoparticles: A bibliometric analysis”. Toxicol Ind Health 2019; 35: 399–402. [DOI] [PubMed] [Google Scholar]
- 14.Fu HZ, Ho YS. Top cited articles in adsorption research using Y-index. Res Evaluat 2014; 23: 12–20. [Google Scholar]
- 15.Ho YS, Siu E, Chuang KY. A bibliometric analysis of dengue-related publications in the Science Citation Index Expanded. Future Virol 2016; 11: 631–648. [Google Scholar]
- 16.Gutman SA, Brown T, Ho YS. A bibliometric analysis of highly cited and high impact occupational therapy publications by American authors. Occup Ther Health Care 2017; 31: 167–187. DOI: 10.1080/07380577.2017.1326192. [DOI] [PubMed] [Google Scholar]
- 17.Kontoyiannis D, Pasparakis M, Pizarro TT, et al. Impaired on/off regulation of TNF biosynthesis in mice lacking TNF AU-rich elements: implications for joint and gut-associated immunopathologies. Immunity 1999; 10: 387–398. [DOI] [PubMed] [Google Scholar]
- 18.Panés J, García-Olmo D, Van Assche G, et al. Expanded allogeneic adipose-derived mesenchymal stem cells (Cx601) for complex perianal fistulas in Crohn's disease: a phase 3 randomised, double-blind controlled trial. Lancet 2016; 388: 1281–1290. DOI: 10.1016/S0140-6736(16)31203-X. [DOI] [PubMed] [Google Scholar]
- 19.Kaplan GG. The global burden of IBD: from 2015 to 2025. Nat Rev Gastroenterol Hepatol 2015; 12: 720–727. DOI: 10.1038/nrgastro.2015.150. [DOI] [PubMed] [Google Scholar]
- 20.Kaplan GG, Ng SC. Understanding and preventing the global increase of inflammatory bowel disease. Gastroenterology 2017; 152: 313–321.e2. DOI: 10.1053/j.gastro.2016.10.020. [DOI] [PubMed] [Google Scholar]
- 21.Molodecky NA, Soon IS, Rabi DM, et al. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology 2012; 142: 46–54.e42. DOI: 10.1053/j.gastro.2011.10.001. [DOI] [PubMed] [Google Scholar]
- 22.Ho YS, Fu HZ. Mapping of metal-organic frameworks publications: A bibliometric analysis. Inorg Chem Commun 2016; 73: 174–182. [Google Scholar]
- 23.Li LL, Ding GH, Feng N, et al. Global stem cell research trend: Bibliometric analysis as a tool for mapping of trends from 1991 to 2006. Scientometrics 2009; 80: 39–58. [Google Scholar]
- 24.Brandt JS, Downing AC, Howard DL, et al. Citation classics in obstetrics and gynecology: The 100 most frequently cited journal articles in the last 50 years. Am J Obstet Gynecol 2010; 203: 355.e1-7. [DOI] [PubMed] [Google Scholar]
- 25.Van Deen WK, Oikonomopoulos A, Hommes DW. Stem cell therapy in inflammatory bowel disease: which, when and how? Curr Opin Gastroenterol 2013; 29: 384–390. DOI: 10.1097/MOG.0b013e328361f763. [DOI] [PubMed] [Google Scholar]
- 26.Randhawa PK, Singh K, Singh N, et al. A review on chemical-induced inflammatory bowel disease models in rodents. Korean J Physiol Pharmacol 2014; 18: 279–288. DOI: 10.4196/kjpp.2014.18.4.279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Romieu-Mourez R, Coutu DL, Galipeau J. The immune plasticity of mesenchymal stromal cells from mice and men: concordances and discrepancies. Front Biosci (Elite Ed) 2012; 4: 824–837. [DOI] [PubMed] [Google Scholar]
- 28.Chinnadurai R, Ng S, Velu V, et al. Challenges in animal modelling of mesenchymal stromal cell therapy for inflammatory bowel disease. World J Gastroenterol 2015; 21: 4779–4787. DOI: 10.3748/wjg.v21.i16.4779. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Hawkey CJ, Snowden JA, Lobo A, et al. Stem cell transplantation for inflammatory bowel disease: practical and ethical issues. Gut 2000; 46: 869–872. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Bartholomew A, Sturgeon C, Siatskas M, et al. Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo. Exp Hematol 2002; 30: 42–48. [DOI] [PubMed] [Google Scholar]
- 31.Di Nicola M, Carlo-Stella C, Magni M, et al. Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli. Blood 2002; 99: 3838–3843. DOI: 10.1182/blood.v99.10.3838. [DOI] [PubMed] [Google Scholar]
- 32.Zangi L, Margalit R, Reich-Zeliger S, et al. Direct imaging of immune rejection and memory induction by allogeneic mesenchymal stromal cells. Stem Cells 2009; 27: 2865–2874. DOI: 10.1002/stem.217. [DOI] [PubMed] [Google Scholar]
- 33.Gonzalez-Rey E, Anderson P, Gonzalez MA, et al. Human adult stem cells derived from adipose tissue protect against experimental colitis and sepsis. Gut 2009; 58: 929–939. [DOI] [PubMed] [Google Scholar]
- 34.Duijvestein M, Molendijk I, Roelofs H, et al. Mesenchymal stromal cell function is not affected by drugs used in the treatment of inflammatory bowel disease. Cytotherapy 2011; 13: 1066–1073. DOI: 10.3109/14653249.2011.597379. [DOI] [PubMed] [Google Scholar]
- 35.Holmberg FEO, Pedersen J, Jorgensen P, et al. Intestinal barrier integrity and inflammatory bowel disease: Stem cell-based approaches to regenerate the barrier. J Tissue Eng Regen Med 2018; 12: 923–935. DOI: 10.1002/term.2506. [DOI] [PubMed] [Google Scholar]
- 36.Wehkamp J, Salzman NH, Porter E, et al. Reduced Paneth cell alpha-defensins in ileal Crohn’s disease. Proc Natl Acad Sci USA 2005; 102: 18129–18134. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Wehkamp J, Harder J, Weichenthal M, et al. NOD2 (CARD15) mutations in Crohn’s disease are associated with diminished mucosal alpha-defensin expression. Gut 2004; 53: 1658–1664. DOI: 10.1136/gut.2003.032805. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Peyrin-Biroulet L, Beisner J, Wang G, et al. Peroxisome proliferator-activated receptor gamma activation is required for maintenance of innate antimicrobial immunity in the colon. Proc Natl Acad Sci USA 2010; 107: 8772–8777. DOI: 10.1073/pnas.0905745107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Mccormick DA, Horton LWL, Mee AS. Mucin depletion in inflammatory bowel disease. J Clin Pathol 1990; 43: 143–146. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Pullan RD, Thomas GA, Rhodes M, et al. Thickness of adherent mucus gel on colonic mucosa in humans and its relevance to colitis. Gut 1990; 35: 353–359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Sato T, Stange DE, Ferrante M, et al. Long-term expansion of epithelial organoids from human colon, adenoma, adenocarcinoma, and Barrett's epithelium. Gastroenterology 2011; 141: 1762–1772. DOI: 10.1053/j.gastro.2011.07.050. [DOI] [PubMed] [Google Scholar]
- 42.Spence JR, Mayhew CN, Rankin SA, et al. Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro. Nature 2011; 470: 105–109. DOI: 10.1038/nature09691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Watson CL, Mahe MM, Munera J, et al. An in vivo model of human small intestine using pluripotent stem cells. Nat Med 2014; 20: 1310–1314. DOI: 10.1038/nm.3737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Zhao M, Burisch J. Impact of genes and the environment on the pathogenesis and disease course of inflammatory bowel disease. Dig Dis Sci 2019; 64: 1759–1769. DOI: 10.1007/s10620-019-05648-w. [DOI] [PubMed] [Google Scholar]
- 45.Cleynen I, Gonzalez JR, Figueroa C, et al. Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project. Gut 2013; 62: 1556–1565. DOI: 10.1136/gutjnl-2011-300777. [DOI] [PubMed] [Google Scholar]
- 46.Helio T. CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease. Gut 2003; 52: 558–562. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Bank S, Skytt Andersen P, Burisch J, et al. Polymorphisms in the inflammatory pathway genes TLR2, TLR4, TLR9, LY96, NFKBIA, NFKB1, TNFA, TNFRSF1A, IL6R, IL10, IL23R, PTPN22, and PPARG are associated with susceptibility of inflammatory bowel disease in a Danish cohort. PLoS One 2014; 9: e98815. DOI: 10.1371/journal.pone.0098815. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Weersma RK, Zhernakova A, Nolte IM, et al. ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands. Am J Gastroenterol 2008; 103: 621–627. DOI: 10.1111/j.1572-0241.2007.01660.x. [DOI] [PubMed] [Google Scholar]
- 49.Nguyen DD, Muthupalani S, Goettel JA, et al. Colitis and colon cancer in WASP-deficient mice require helicobacter species. Inflamm Bowel Dis 2013; 19: 2041–2050. DOI: 10.1097/MIB.0b013e318295fd8f. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Pan W, Jian L, Liu T. Grey system theory trends from 1991 to 2018: a bibliometric analysis and visualization. Scientometrics 2019; 121: 1407–1434. DOI: 10.1007/s11192-019-03256-z. [Google Scholar]
- 51.Buonocore S, Ahern PP, Uhlig HH, et al. Innate lymphoid cells drive interleukin-23-dependent innate intestinal pathology. Nature 2010; 464: 1371–1375. DOI: 10.1038/nature08949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Hermiston ML, Gordon JI. Inflammatory bowel disease and adenomas in mice expressing a dominant negative N-cadherin. Science 1995; 270: 1203–1207. [DOI] [PubMed] [Google Scholar]
- 53.García-Olmo D, García-Arranz M, Herreros D, et al. A phase I clinical trial of the treatment of Crohn’s fistula by adipose mesenchymal stem cell transplantation. Dis Colon Rectum 2005; 48: 1416–1423. [DOI] [PubMed] [Google Scholar]
- 54.Mombaerts P, Mizoguchi E, Grusby MJ, et al. Spontaneous development of inflammatory bowel disease in T cell receptor mutant mice. Cell 1993; 75: 274–282. [DOI] [PubMed] [Google Scholar]
- 55.García-Olmo D, Herreros D, Pascual I, et al. Expanded adipose-derived stem cells for the treatment of complex perianal fistula: a phase II clinical trial. Dis Colon Rectum 2009; 52: 79–86. DOI: 10.1007/DCR.0b013e3181973487. [DOI] [PubMed] [Google Scholar]
- 56.Worthey EA, Mayer AN, Syverson GD, et al. Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease. Genet Med 2011; 13: 255–262. DOI: 10.1097/GIM.0b013e3182088158. [DOI] [PubMed] [Google Scholar]
- 57.Allen IC, TeKippe EM, Woodford R-MT, et al. The NLRP3 inflammasome functions as a negative regulator of tumorigenesis during colitis-associated cancer. The Journal of experimental medicine 2010; 207: 1045–1056. DOI: 10.1084/jem.20100050. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Duijvestein M, Vos ACW, Roelofs H, et al. Autologous bone marrow-derived mesenchymal stromal cell treatment for refractory luminal Crohn’s disease: results of a phase I study. Gut 2010; 59: 1662–1669. DOI: 10.1136/gut.2010.215152. [DOI] [PubMed] [Google Scholar]
- 59.West NR, Hegazy AN, Owens BMJ, et al. Oncostatin M drives intestinal inflammation and predicts response to tumor necrosis factor-neutralizing therapy in patients with inflammatory bowel disease. Nature medicine 2017; 23: 579–589. DOI: 10.1038/nm.4307. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Onengut-Gumuscu S, Chen W-M, Burren O, et al. Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. Nature genetics 2015; 47: 381–386. DOI: 10.1038/ng.3245. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Panés J, García-Olmo D, Van Assche G, et al. Long-term efficacy and safety of stem cell therapy (Cx601) for complex perianal fistulas in patients with Crohn’s disease. Gastroenterology 2018; 154: 1334–1342.e4. DOI: 10.1053/j.gastro.2017.12.020. [DOI] [PubMed] [Google Scholar]
- 62.González MA, Gonzalez-Rey E, Rico L, et al. Adipose-derived mesenchymal stem cells alleviate experimental colitis by inhibiting inflammatory and autoimmune responses. Gastroenterology 2009; 136: 978–989. DOI: 10.1053/j.gastro.2008.11.041. [DOI] [PubMed] [Google Scholar]
- 63.Ciccocioppo R, Bernardo ME, Sgarella A, et al. Autologous bone marrow-derived mesenchymal stromal cells in the treatment of fistulising Crohn’s disease. Gut 2011; 60: 788–798. DOI: 10.1136/gut.2010.214841. [DOI] [PubMed] [Google Scholar]