The DOI matches its Crossref record; 78 of the 79 references it cites were found in a registry or an index.
Butyrate and other short-chain fatty acids as modulators of immunity: what relevance for health?
Abstract
PURPOSE OF REVIEW: High-fiber diets have been shown to reduce plasma concentrations of inflammation markers. Increased production of fermentation-derived short-chain fatty acids (SCFAs) is one of the factors that could exert these positive effects. This review examines the effects of SCFAs on immune cells and discusses the relevance of their effects on systemic inflammation, as frequently seen in obesity. RECENT FINDINGS: SCFAs have been shown to reduce chemotaxis and cell adhesion; this effect is dependent on type and concentration of SCFA. In spite of conflicting results, especially butyrate seems to have an anti-inflammatory effect, mediated by signaling pathways like nuclear factor-κB and inhibition of histone deacetylase. The discrepancies in the results could be explained by differences in cell types used and their proliferative and differentiation status. SUMMARY: SCFAs show anti-inflammatory effects and seem to have the potency to prevent infiltration of immune cells from the bloodstream in, for example, the adipose tissue. In addition, their ability to inhibit the proliferation and activation of T cells and to prevent adhesion of antigen-presenting cells could be important as it recently has been shown that obesity-associated inflammation might be antigen-dependent. More studies with concentrations in micromolar range are needed to approach more physiological concentrations.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Other studies have shown that SCFA, particularly acetate and butyrate, can act as anti-inflammatory agents and have been shown to be effective in inhibiting the production of pro-inflammatory cytokines and maintaining intestinal barrier immune function [255].”
From Lactic Acid Bacteria in Raw-Milk Cheeses: From Starter Cultures to Probiotic Functions (2022) · cites this paper as [255]
Citations
Cites
Ridker, P. M., Hennekens, C. H., Buring, J. E., & Rifai, N. (2000) · New England Journal of Medicine · doi:10.1056/nejm200003233421202 · Cited by 5,850
C-Reactive Protein, Interleukin 6, and Risk of Developing Type 2 Diabetes Mellitus
Pradhan, A. D. (2001) · JAMA · doi:10.1001/jama.286.3.327 · Cited by 4,433
Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43
Maslowski, K. M., Vieira, A. T., Ng, A., Kranich, J., Sierro, F., Yu, D., Schilter, H. C., Rolph, M. S., Mackay, F., Artis, D., et al. (2009) · Nature · doi:10.1038/nature08530 · Cited by 3,241
Short chain fatty acids in human large intestine, portal, hepatic and venous blood
Cummings, J. H., Pomare, E. W., Branch, W. J., Naylor, C. P., & Macfarlane, G. T. (1987) · Gut · doi:10.1136/gut.28.10.1221 · Cited by 3,119
Macrophages, inflammation, and insulin resistance
Olefsky, J. M., & Glass, C. K. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135846 · Cited by 2,733
Brown, A. J., Goldsworthy, S. M., Barnes, A. A., Eilert, M. M., Tcheang, L., Daniels, D., Muir, A. I., Wigglesworth, M. J., Kinghorn, I., Fraser, N. J., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211609200 · Cited by 2,409
Nishimura, S., Manabe, I., Nagasaki, M., Eto, K., Yamashita, H., Ohsugi, M., Otsu, M., Hara, K., Ueki, K., Sugiura, S., et al. (2009) · Nature Medicine · doi:10.1038/nm.1964 · Cited by 2,230
Feuerer, M., Herrero, L., Cipolletta, D., Naaz, A., Wong, J., Nayer, A., Lee, J., Goldfine, A. B., Benoist, C., Shoelson, S., et al. (2009) · Nature Medicine · doi:10.1038/nm.2002 · Cited by 2,145
Le Poul, E., Loison, C., Struyf, S., Springael, J.-Y., Lannoy, V., Decobecq, M.-E., Brezillon, S., Dupriez, V., Vassart, G., Van Damme, J., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301403200 · Cited by 1,651
Inhibition of Histone Deacetylase Activity by Butyrate
Davie, J. R. (2003) · The Journal of Nutrition · doi:10.1093/jn/133.7.2485s · Cited by 1,515
Research works printed but not linked: 5
- Schley, 2002, Br J Nutr, 87, S221, 10.1079/BJN/2002541 · DOI
- Zapolska-Downar, 2009, J Physiol Pharmacol, 60, 123
- Kouraklis, 2006, Oncol Rep, 15, 489
- Chung, 1985, Cancer Res, 45, 2976
- Kruh, 1982, Mol Cell Biochem, 42, 65
Cited by
Sorted by citations
Role of the microbiota in immunity and inflammation.
Belkaid, Y., & Hand, T. W. (2014) · Cell · doi:10.1016/j.cell.2014.03.011 · Cited by 5,385
Potential beneficial effects of butyrate in intestinal and extraintestinal diseases
Canani, R. B. (2011) · World Journal of Gastroenterology · doi:10.3748/wjg.v17.i12.1519 · Cited by 1,381
Butyrate: A Double-Edged Sword for Health?
Liu, H., Wang, J., He, T., Becker, S. R., Zhang, G., Li, D., & Ma, X. (2018) · Advances in Nutrition · doi:10.1093/advances/nmx009 · Cited by 1,184
Gut Microbiota and Immune System Interactions
Yoo, J. Y., Groer, M. E., Dutra, S. V. O., Sarkar, A., & McSkimming, D. I. (2020) · Microorganisms · doi:10.3390/microorganisms8101587 · Cited by 1,110
The Gut Microbiota and Alzheimer’s Disease
Jiang, C., Li, G., Huang, P., Liu, Z., & Zhao, B. (2017) · Journal of Alzheimer's Disease · doi:10.3233/jad-161141 · Cited by 852
Shifting the balance: antibiotic effects on host–microbiota mutualism
Willing, B. P., Russell, S. L., & Finlay, B. B. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2536 · Cited by 747
The gut microbiome as a major regulator of the gut-skin axis
Salem, I., Ramser, A., Isham, N., & Ghannoum, M. A. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01459 · Cited by 707
Microbiota of the chicken gastrointestinal tract: influence on health, productivity and disease
Stanley, D., Hughes, R., & Moore, R. J. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5646-2 · Cited by 665
Verdam, F. J., Fuentes, S., de Jonge, C., Zoetendal, E. G., Erbil, R., Greve, J. W., Buurman, W. A., de Vos, W. M., & Rensen, S. S. (2013) · Obesity · doi:10.1002/oby.20466 · Cited by 587
Impact of Diet-Modulated Butyrate Production on Intestinal Barrier Function and Inflammation
Bach Knudsen, K. E., Lærke, H. N., Hedemann, M. S., Nielsen, T. S., Ingerslev, A. K., Gundelund Nielsen, D. S., Theil, P. K., Purup, S., Hald, S., Schioldan, A. G., et al. (2018) · Nutrients · doi:10.3390/nu10101499 · Cited by 572
The role of adipose tissue immune cells in obesity and low-grade inflammation
Mraz, M., & Haluzik, M. (2014) · Journal of Endocrinology · doi:10.1530/joe-14-0283 · Cited by 543
Nondigestible carbohydrates, butyrate, and butyrate-producing bacteria
Fu, X., Liu, Z., Zhu, C., Mou, H., & Kong, Q. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1542587 · Cited by 497
Systemic short chain fatty acids limit antitumor effect of CTLA-4 blockade in hosts with cancer
Coutzac, C., Jouniaux, J.-M., Paci, A., Schmidt, J., Mallardo, D., Seck, A., Asvatourian, V., Cassard, L., Saulnier, P., Lacroix, L., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16079-x · Cited by 513
Position of the Academy of Nutrition and Dietetics: Health implications of dietary fiber
Dahl, W. J., & Stewart, M. L. (2015) · Journal of the Academy of Nutrition and Dietetics · doi:10.1016/j.jand.2015.09.003 · Cited by 471
Implications of butyrate and its derivatives for gut health and animal production
Bedford, A., & Gong, J. (2017) · Animal nutrition · doi:10.1016/j.aninu.2017.08.010 · Cited by 482
Regulation of lung immunity and host defense by the intestinal microbiota
Samuelson, D. R., Welsh, D. A., & Shellito, J. E. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01085 · Cited by 447
The epigenetic effects of butyrate: potential therapeutic implications for clinical practice
Berni Canani, R., Di Costanzo, M., & Leone, L. (2012) · Clinical Epigenetics · doi:10.1186/1868-7083-4-4 · Cited by 431
Factors Influencing the Gut Microbiota, Inflammation, and Type 2 Diabetes
Li, W., & Duffy, A. J. (2017) · Journal of Nutrition · doi:10.3945/jn.116.240754 · Cited by 433
Role of microbiota-derived short-chain fatty acids in cancer development and prevention
Mirzaei, R., Afaghi, A., Babakhani, S., Sohrabi, M., Hosseini‐Fard, S. R., Babolhavaeji, K., Akbari, S. K. A., Yousefimashouf, R., & Karampoor, S. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111619 · Cited by 412
Breast cancer in postmenopausal women is associated with an altered gut metagenome
Zhu, J., Liao, M., Yao, Z., Liang, W., Li, Q., Liu, J., Yang, H., Ji, Y., Wei, W., Tan, A., et al. (2018) · Microbiome · doi:10.1186/s40168-018-0515-3 · Cited by 377
Human microbiomes and their roles in dysbiosis, common diseases, and novel therapeutic approaches
Belizário, J. E., & Napolitano, M. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01050 · Cited by 389
Gut–organ axis: a microbial outreach and networking
Ahlawat, S., Asha, A., & Sharma, K. K. (2020) · Letters in Applied Microbiology · doi:10.1111/lam.13333 · Cited by 369
Gut Microbiome Dysbiosis and Immunometabolism: New Frontiers for Treatment of Metabolic Diseases
Belizário, J. E., Faintuch, J., & Garay-Malpartida, M. (2018) · Mediators of Inflammation · doi:10.1155/2018/2037838 · Cited by 341
Li, M., van Esch, B. C. A. M., Henricks, P. A. J., Folkerts, G., & Garssen, J. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00533 · Cited by 353
Emergent Sources of Prebiotics: Seaweeds and Microalgae
De Jesus Raposo, M., De Morais, A., & De Morais, R. (2016) · Marine Drugs · doi:10.3390/md14020027 · Cited by 331
Młynarska, E., Czarnik, W., Kurys, N., Jędraszak, W., Majchrowicz, G., Prusinowski, F., Stabrawa, M., Rysz, J., & Franczyk, B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26031094 · Cited by 451
Regulation of the effector function of CD8+ T cells by gut microbiota-derived metabolite butyrate
Luu, M., Weigand, K., Wedi, F., Breidenbend, C., Leister, H., Pautz, S., Adhikary, T., & Visekruna, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-32860-x · Cited by 344
Puddu, A., Sanguineti, R., Montecucco, F., & Viviani, G. L. (2014) · Mediators of Inflammation · doi:10.1155/2014/162021 · Cited by 358
Marizzoni, M., Cattaneo, A., Mirabelli, P., Festari, C., Lopizzo, N., Nicolosi, V., Mombelli, E., Mazzelli, M., Luongo, D., Naviglio, D., et al. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200306 · Cited by 351
Tong, L., Wang, Y., Wang, Z.-B., Liu, W., Sun, S., Li, L., Su, D., & Zhang, L. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2016.00253 · Cited by 334
Shen, Y., Xu, J., Li, Z., Huang, Y., Yuan, Y., Wang, J., Zhang, M., Hu, S., & Liang, Y. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.01.002 · Cited by 328
Skin Barrier Function and the Microbiome
Lee, H.-J., & Kim, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113071 · Cited by 317
Alex, S., Lange, K., Amolo, T., Grinstead, J. S., Haakonsson, A. K., Szalowska, E., Koppen, A., Mudde, K., Haenen, D., Al-Lahham, S., et al. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00858-12 · Cited by 307
Iraporda, C., Errea, A. J., Romanin, D., Cayet, D., Pereyra, E. N., Pignataro, O. P., Sirard, J., Garrote, G. L., Abraham, A. G., & Rumbo, M. (2015) · Immunobiology · doi:10.1016/j.imbio.2015.06.004 · Cited by 284
Lactic Acid Bacteria in Raw-Milk Cheeses: From Starter Cultures to Probiotic Functions
Coelho, M. C., Malcata, F. X., & Silva, C. C. G. (2022) · Foods · doi:10.3390/foods11152276 · Cited by 276
“Other studies have shown that SCFA, particularly acetate and butyrate, can act as anti-inflammatory agents and have been shown to be effective in inhibiting the production of pro-inflammatory cytokines and maintaining intestinal barrier immune function [255].”
Voluntary and forced exercise differentially alters the gut microbiome in C57BL/6J mice
Allen, J. M., Berg Miller, M. E., Pence, B. D., Whitlock, K., Nehra, V., Gaskins, H. R., White, B. A., Fryer, J. D., & Woods, J. A. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01077.2014 · Cited by 266
Is butyrate the link between diet, intestinal microbiota and obesity-related metabolic diseases?
Brahe, L. K., Astrup, A., & Larsen, L. H. (2013) · Obesity Reviews · doi:10.1111/obr.12068 · Cited by 264
Belizário, J. E., & Faintuch, J. (2018) · Experientia supplementum · doi:10.1007/978-3-319-74932-7_13 · Cited by 270
Conterno, L., Fava, F., Viola, R., & Tuohy, K. M. (2011) · Genes & Nutrition · doi:10.1007/s12263-011-0230-1 · Cited by 253
Liu, T., Li, J., Liu, Y., Xiao, N., Suo, H., Xie, K., Yang, C., & Wu, C. (2012) · Inflammation · doi:10.1007/s10753-012-9484-z · Cited by 248
Role of Fatty Acids in Milk Fat and the Influence of Selected Factors on Their Variability—A Review
Hanuš, O., Samková, E., Křížová, L., Hasoňová, L., & Kala, R. (2018) · Molecules · doi:10.3390/molecules23071636 · Cited by 259
Elamin, E. E., Masclee, A., Jan, D., Pieters, H., & Jonkers, D. M. A. E. (2013) · Journal of Nutrition · doi:10.3945/jn.113.179549 · Cited by 237
Ohira, H., Fujioka, Y., Katagiri, C., Mamoto, R., Aoyama-Ishikawa, M., Amako, K., Izumi, Y., Nishiumi, S., Yoshida, M., Usami, M., et al. (2013) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.15065 · Cited by 242
Propionic acid affects immune status and metabolism in adipose tissue from overweight subjects
Al-Lahham, S., Roelofsen, H., Rezaee, F., Weening, D., Hoek, A., Vonk, R. J., & Venema, K. (2011) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2011.02590.x · Cited by 233
β-Glucan in Foods and Its Physiological Functions
Nakashima, A., Yamada, K., Iwata, O., Sugimoto, R., Atsuji, K., OGAWA, T., Ishibashi-Ohgo, N., & Suzuki, K. (2018) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.64.8 · Cited by 231
Functional analysis of colonic bacterial metabolism: relevant to health?
Hamer, H. M., Preter, V. D., Windey, K., & Verbeke, K. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00048.2011 · Cited by 221
Progress and perspectives of short‐chain fatty acids in aquaculture
Tran, N. T., Li, Z., Wang, S., Zheng, H., Aweya, J. J., Wen, X., & Li, S. (2018) · Reviews in Aquaculture · doi:10.1111/raq.12317 · Cited by 218
Selective Manipulation of the Gut Microbiota Improves Immune Status in Vertebrates
Montalban‐Arques, A., Schryver, P. D., Bossier, P., Gorkiewicz, G., Mulero, V., Gatlin, D. M., & Galindo‐Villegas, J. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00512 · Cited by 222
Alterations of the Skin and Gut Microbiome in Psoriasis and Psoriatic Arthritis
Olejniczak‐Staruch, I., Ciążyńska, M. A., Sobolewska-Sztychny, D., Narbutt, J., Skibińska, M., & Lesiak, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083998 · Cited by 234
Li, K., Zhang, L., Xue, J., Yang, X., Dong, X., Sha, L., Lei, H., Zhang, X., Zhu, L., Wang, Z., et al. (2019) · Food & Function · doi:10.1039/c8fo02265h · Cited by 210
Immune Modulation by Different Types of β2→1-Fructans Is Toll-Like Receptor Dependent
Vogt, L., Ramasamy, U. S., Meyer, D., Pullens, G., Venema, K., Faas, M. M., Schols, H. A., & de Vos, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068367 · Cited by 200
Asarat, M., Apostolopoulos, V., Vasiljevic, T., & Donkor, O. N. (2016) · Immunological Investigations · doi:10.3109/08820139.2015.1122613 · Cited by 204
RetractedImmunological properties of inulin-type fructans
Vogt, L., Meyer, D., Pullens, G., Faas, M., Smelt, M., Venema, K., Ramasamy, U., Schols, H. A., & De Vos, P. (2015) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2012.656772 · Cited by 195
Acetate and Butyrate Improve β-cell Metabolism and Mitochondrial Respiration under Oxidative Stress
Hu, S., Kuwabara, R., de Haan, B. J., Smink, A. M., & de Vos, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041542 · Cited by 191
Benefits of Dietary Butyric Acid, Sodium Butyrate, and Their Protected Forms in Aquafeeds: A Review
Abdel‐Latif, H. M. R., Abdel‐Tawwab, M., Dawood, M. A. O., Menanteau‐Ledouble, S., & El‐Matbouli, M. (2020) · Reviews in Fisheries Science & Aquaculture · doi:10.1080/23308249.2020.1758899 · Cited by 192
Modulation of immune homeostasis by commensal bacteria
Ivanov, I. I., & Littman, D. R. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2010.12.003 · Cited by 188
Zhang, Z., Xu, M., Wang, L., Gu, W., Li, X., Han, Z., Fu, X., Wang, X., Xu, L., & Su, Z. (2023) · Environment International · doi:10.1016/j.envint.2023.108353 · Cited by 193
An insight into intestinal mucosal microbiota disruption after stroke
Stanley, D., Moore, R. J., & Wong, C. H. Y. (2018) · Scientific Reports · doi:10.1038/s41598-017-18904-8 · Cited by 174
Chen, L., Li, J., Zhu, W., Kuang, Y., Liu, T., Zhang, W., Chen, X., & Peng, C. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.589726 · Cited by 175
The microbiota, immunoregulation, and mental health: implications for public health
Lowry, C. A., Smith, D. G., Siebler, P. H., Schmidt, D., Stamper, C. E., Hassell, J. E., Yamashita, P. S., Fox, J. H., Reber, S. O., Brenner, L. A., et al. (2016) · Current Environmental Health Reports · doi:10.1007/s40572-016-0100-5 · Cited by 172
Mirmonsef, P., Zariffard, M. R., Gilbert, D. Z., Makinde, H. M., LANDAY, A. L., & Spear, G. T. (2011) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2011.01089.x · Cited by 165
Celiberto, L. S., Graef, F. A., Healey, G. R., Bosman, E. S., Jacobson, K., Sly, L. M., & Vallance, B. A. (2018) · Immunology · doi:10.1111/imm.12939 · Cited by 167
Ashique, S., Rubis, G. D., Sirohi, E., Mishra, N., Rihan, M., Garg, A., Reyes, R.-J., Manandhar, B., Bhatt, S., Jha, N. K., et al. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.110231 · Cited by 177
The role of short-chain fatty acids in inflammatory skin diseases
Xiao, X., Hu, X., Yao, J., Cao, W., Zou, Z., Wang, L., Qin, H., Zhong, D., Li, Y., Xue, P., et al. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1083432 · Cited by 183
Infectious Threats, the Intestinal Barrier, and Its Trojan Horse: Dysbiosis
Iacob, S. A., & Iacob, D. G. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01676 · Cited by 158
van Deuren, T., Blaak, E. E., & Canfora, E. E. (2022) · Obesity Reviews · doi:10.1111/obr.13498 · Cited by 166
Modulation of the gut microbiota by prebiotic fibres and bacteriocins
Umu, Ö. C. O., Rudi, K., & Diep, D. B. (2017) · Microbial Ecology in Health and Disease · doi:10.1080/16512235.2017.1348886 · Cited by 159
Gut bacterial diversity of the tribes of India and comparison with the worldwide data
Dehingia, M., Kanchal, T., Talukdar, N. C., Talukdar, R., Reddy, D. N., Mande, S. S., Deka, M., & Khan, M. R. (2015) · Scientific Reports · doi:10.1038/srep18563 · Cited by 147
Role of Porphyromonas gingivalis in oral and orodigestive squamous cell carcinoma
Lamont, R. J., Fitzsimonds, Z. R., Wang, H., & Gao, S. (2022) · Periodontology 2000 · doi:10.1111/prd.12425 · Cited by 147
Xie, M., Zhou, W., Xie, Y., Yu, L., Zhang, Z., Yang, Y., Olsen, R. E., Ran, C., & Zhou, Z. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2021.736943 · Cited by 142
Chuang, S., Norat, T., Murphy, N., Olsen, A., Tjønneland, A. M., Overvad, K., Boutron‐Ruault, M., Perquier, F., Dartois, L., Kaaks, R., et al. (2012) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.111.028415 · Cited by 142
Lokesh, J., Fernandes, J. M. O., Korsnes, K., Bergh, Ø., Brinchmann, M. F., & Kiron, V. (2012) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2012.06.017 · Cited by 145
Su, B., Liu, H., Li, J., Sunli, Y., Liu, B., Liu, D., Zhang, P., & Meng, X. (2014) · Journal of Diabetes · doi:10.1111/1753-0407.12232 · Cited by 136
Xiong, H., Guo, B., Gan, Z.-S., Song, D., Lu, Z., Yi, H., Wu, Y., Wang, Y., & Du, H. (2016) · Scientific Reports · doi:10.1038/srep27070 · Cited by 139
Microbial programming of health and disease starts during fetal life
Koleva, P. T., Kim, J., Scott, J. A., & Kozyrskyj, A. L. (2015) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21117 · Cited by 130
Postbiotics: facts and open questions. A position paper on the need for a consensus definition
Collado, M. C., Vinderola, G., & Salminen, S. (2019) · Beneficial Microbes · doi:10.3920/bm2019.0015 · Cited by 132
Gut microbiota restoration through fecal microbiota transplantation: a new atopic dermatitis therapy
Kim, J., Kim, K., & Kim, W. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00627-6 · Cited by 135
Brugman, S., Ikeda‐Ohtsubo, W., Braber, S., Folkerts, G., Pieterse, C. M. J., & Bakker, P. A. H. M. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00080 · Cited by 133
Microbiota and dietary interactions – an update to the hygiene hypothesis?
Frei, R., Lauener, R. P., Crameri, R., & O’Mahony, L. (2012) · Allergy · doi:10.1111/j.1398-9995.2011.02783.x · Cited by 131
Synthetic microbial communities (SynComs) of the human gut: design, assembly, and applications
van Leeuwen, P. T., Brul, S., Zhang, J., & Wortel, M. T. (2023) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuad012 · Cited by 128
Sun, Y.-Y., Li, M., Li, Y.-Y., Li, L.-X., Zhai, W.-Z., Wang, P., Yang, X.-X., Gu, X., Song, L.-J., Li, Z., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-21241-z · Cited by 126
The intestinal microbiota and host immune interactions in the critically ill
Schuijt, T. J., van der Poll, T., de Vos, W. M., & Wiersinga, W. J. (2013) · Trends in Microbiology · doi:10.1016/j.tim.2013.02.001 · Cited by 123
Histamine receptor 2 modifies dendritic cell responses to microbial ligands
Frei, R., Ferstl, R., Konieczna, P., Ziegler, M., Simon, T., Rugeles, T. M., Mailand, S., Watanabe, T., Lauener, R. P., Akdiş, C. A., et al. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.01.013 · Cited by 123
Intestinal Flora as a Potential Strategy to Fight SARS-CoV-2 Infection
He, L., Ren, L., Li, J., Wu, Y.-N., Li, X., & Zhang, L. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01388 · Cited by 135
Geraylou, Z., Souffreau, C., Rurangwa, E., D’hondt, S., Callewaert, L., Courtin, C. M., Delcour, J. A., Buyse, J. G., & Ollevier, F. (2012) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2012.06.010 · Cited by 121
Alterations of fecal bacterial communities in patients with lung cancer.
Zhang, W., Zhao, S., Luo, J., Dong, X., Hao, Y., Li, H., Shan, L., Zhou, Y., Shi, H., Zhang, Z.-Y., et al. (2018) · Europe PMC (PubMed Central) · Cited by 123
Young, R. P., Hopkins, R. J., & Marsland, B. J. (2015) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2015-0250ps · Cited by 119
Liu, H., Rocha, C. S., Dandekar, S., & Wan, Y. Y. (2016) · Journal of Hepatology · doi:10.1016/j.jhep.2015.09.022 · Cited by 120
Vogt, L. M., Meyer, D., Pullens, G., Faas, M. M., Venema, K., Ramasamy, U. S., Schols, H. A., & de Vos, P. (2014) · Journal of Nutrition · doi:10.3945/jn.114.191643 · Cited by 114
Qiao, Y., Zhang, K., Zhang, Z., Zhang, C., Sun, Y., & Feng, Z. (2022) · Food Research International · doi:10.1016/j.foodres.2022.111575 · Cited by 113
Bortoluzzi, C., Pedroso, A. A., Mallo, J. J., Puyalto, M., Kim, W. K., & Applegate, T. J. (2017) · Poultry Science · doi:10.3382/ps/pex218 · Cited by 118
Li, G., Yao, W., & Jiang, H. (2014) · Journal of Nutrition · doi:10.3945/jn.114.198531 · Cited by 110
Bai, J., Zhu, Y. G., & Dong, Y. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.10.043 · Cited by 115
Short Chain Fatty Acids, pancreatic dysfunction and type 2 diabetes
Mandaliya, D. K., & Seshadri, S. (2019) · Pancreatology · doi:10.1016/j.pan.2019.01.021 · Cited by 112
Association of dietary fibre intake and gut microbiota in adults
Lin, D., Peters, B. A., Friedlander, C., Freiman, H. J., Goedert, J. J., Sinha, R., Miller, G., Bernstein, M. A., Hayes, R. B., & Ahn, J. (2018) · British Journal of Nutrition · doi:10.1017/s0007114518002465 · Cited by 109
Keshari, S., Balasubramaniam, A., Myagmardoloonjin, B., Herr, D. R., Negari, I. P., & Huang, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184477 · Cited by 111
Regulation of dietary fiber on intestinal microorganisms and its effects on animal health
Xue-bing, H., Ma, Y., Ding, S., Fang, J., & Liu, G. (2023) · Animal nutrition · doi:10.1016/j.aninu.2023.06.004 · Cited by 112
Liu, J., Wang, F., Luo, H., Liu, A., Li, K., Li, C., & Jiang, Y. Q. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.11.018 · Cited by 103
Butyrate Modulates Inflammation in Chondrocytes via GPR43 Receptor
Pirozzi, C., Francisco, V., Guida, F., Gómez, R., Lago, F., Pino, J., Meli, R., & Gualillo, O. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000495203 · Cited by 104
Does larch arabinogalactan enhance immune function? A review of mechanistic and clinical trials
Dion, C., Chappuis, E., & Ripoll, C. (2016) · Nutrition & Metabolism · doi:10.1186/s12986-016-0086-x · Cited by 103
Metadata
- Authors
- Meijer, K., de Vos, P., & Priebe, M. G.
- Affiliations
- University Medical Center Groningen (NL)
- Corresponding author
- Priebe, Marion G
- Venue
- Current Opinion in Clinical Nutrition and Metabolic Care
- Published
- 2010-11
- Volume
- 13
- Issue
- 6
- Pages
- 715-721
- ISSN
- 1363-1950 (ISSN-L)
- OpenAlex
- W2109832621
- Cited by
- 443
- References
- 79
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 27 · 2023: 35 · 2022: 48 · 2021: 29 · 2020: 39 · 2019: 32 · 2018: 43 · 2017: 38 · 2016: 32 · 2015: 24 · 2014: 27 · 2013: 21 · 2012: 14
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Opinion in Clinical Nutrition & Metabolic Care (publishedVersion)
- PubMed (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
- Keywords
- short-chain fatty acids, butyrate, immunomodulation, anti-inflammatory activity, systemic inflammation, obesity, high-fiber diet, gut fermentation, chemotaxis, cell adhesion, NF-κB signaling, histone deacetylase inhibition, T cell proliferation, antigen-presenting cells, adipose tissue, inflammatory markers
- MeSH terms
- Anti-Inflammatory Agents, Antigen-Presenting Cells, Butyrates, Cell Adhesion, Chemotaxis, Dietary Fiber, Fatty Acids, Volatile, Fermentation, Humans, Immune System, Immunologic Factors, Obesity, Signal Transduction, Inflammation Mediators
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review