Articoli di riviste: "Oral tolerance"

1

Faria, Ana M. C., e Howard L. Weiner. "Oral tolerance". Immunological Reviews 206, n. 1 (agosto 2005): 232–59. http://dx.doi.org/10.1111/j.0105-2896.2005.00280.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

2

SMITH, K. M., A. D. EATON, L. M. FINLAYSON e P. GARSIDE. "Oral Tolerance". American Journal of Respiratory and Critical Care Medicine 162, supplement_3 (ottobre 2000): S175—S178. http://dx.doi.org/10.1164/ajrccm.162.supplement_3.15tac7.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

3

Weiner, Howard L., Andre Pires da Cunha, Francisco Quintana e Henry Wu. "Oral tolerance". Immunological Reviews 241, n. 1 (13 aprile 2011): 241–59. http://dx.doi.org/10.1111/j.1600-065x.2011.01017.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

4

Weiner, H. L. "Oral tolerance." Proceedings of the National Academy of Sciences 91, n. 23 (8 novembre 1994): 10762–65. http://dx.doi.org/10.1073/pnas.91.23.10762.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

5

Wu, Henry Yim, e Howard L. Weiner. "Oral Tolerance". Immunologic Research 28, n. 3 (2003): 265–84. http://dx.doi.org/10.1385/ir:28:3:265.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

6

Garside, P., e A. McI Mowat. "Oral tolerance". Seminars in Immunology 13, n. 3 (giugno 2001): 177–85. http://dx.doi.org/10.1006/smim.2001.0310.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

7

Moreau, Caroline, James Trussell, Fabien Gilbert, Nathalie Bajos e Jean Bouyer. "Oral Contraceptive Tolerance". Obstetrics & Gynecology 109, n. 6 (giugno 2007): 1277–85. http://dx.doi.org/10.1097/01.aog.0000260956.61835.6d.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

8

Garside, Paul, e Allan Mcl Mowat. "Mechanisms of Oral Tolerance". Critical Reviews™ in Immunology 17, n. 2 (1997): 119–37. http://dx.doi.org/10.1615/critrevimmunol.v17.i2.10.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

9

Eiks, M. L. "Oral Glucose Tolerance Tests". Diabetes Care 19, n. 3 (1 marzo 1996): 271. http://dx.doi.org/10.2337/diacare.19.3.271a.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

10

Margalit, Maya, e Yaron Ilan. "Oral Tolerance for IBD". American Journal of Gastroenterology 101, n. 12 (dicembre 2006): 2890–91. http://dx.doi.org/10.1111/j.1572-0241.2006.00867_9.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

11

GARSIDE, P., A. McI MOWAT e A. KHORUTS. "Oral tolerance in disease". Gut 44, n. 1 (1 gennaio 1999): 137–42. http://dx.doi.org/10.1136/gut.44.1.137.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

12

Hamad, Ahmad, e Wesley Burks. "Oral tolerance and allergy". Seminars in Immunology 30 (aprile 2017): 28–35. http://dx.doi.org/10.1016/j.smim.2017.07.001.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

13

Commins, Scott P. "Mechanisms of Oral Tolerance". Pediatric Clinics of North America 62, n. 6 (dicembre 2015): 1523–29. http://dx.doi.org/10.1016/j.pcl.2015.07.013.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

14

Greenspoon, Jeffrey S. "Oral Glucose Tolerance Test". Mayo Clinic Proceedings 63, n. 8 (agosto 1988): 838. http://dx.doi.org/10.1016/s0025-6196(12)62371-4.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

15

Tordesillas, Leticia, e M. Cecilia Berin. "Mechanisms of Oral Tolerance". Clinical Reviews in Allergy & Immunology 55, n. 2 (27 febbraio 2018): 107–17. http://dx.doi.org/10.1007/s12016-018-8680-5.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

16

Stanley, Steve. "Oral tolerance of food". Current Allergy and Asthma Reports 2, n. 1 (gennaio 2002): 73–77. http://dx.doi.org/10.1007/s11882-002-0043-9.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

17

Nguyen, Nhan H., Vincent Chak, Katherine Keller, Helen Wu e Sathy V. Balu-Iyer. "Phosphatidylserine-mediated oral tolerance". Cellular Immunology 384 (febbraio 2023): 104660. http://dx.doi.org/10.1016/j.cellimm.2022.104660.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

18

Chung, Yeonseok, Sun-Young Chang e Chang-Yuil Kang. "Kinetic Analysis of Oral Tolerance: Memory Lymphocytes Are Refractory to Oral Tolerance". Journal of Immunology 163, n. 7 (1 ottobre 1999): 3692–98. http://dx.doi.org/10.4049/jimmunol.163.7.3692.

Testo completo

Abstract (sommario):

Abstract Oral administration of soluble Ag before immunization induces peripheral tolerance and is effective in suppressing animal models of autoimmune diseases. Although tolerance induction in primed animals is more clinically relevant, it is not well studied. Therefore, this study was designed to examine the feeding effects on different phases of the immune response. We observed that feeding a single high dose (250 mg) of OVA to OVA-primed BALB/c mice could induce OVA-specific suppression in the Ab production and T cell proliferation only at the naive and the activation phases of the immune response, whereas multiple high doses (100 mg/feed for 10 days) were effective at the effector phase. OVA-specific IL-4 production in culture supernatant was also suppressed in the tolerized groups. However, when the mice had resting memory lymphocytes, even multiple feeding regimens were not effective in tolerance induction, although multiple low doses (1 mg/feed for 10 days) partially suppressed Ab production. This phenomenon was confirmed by adoptive transfer study. Nevertheless, the reactivated memory response was suppressed partially by multiple high doses. Our findings have an important implication for understanding the mechanism of oral tolerance and for the therapeutic applications of oral tolerance to autoimmune diseases.

Gli stili APA, Harvard, Vancouver, ISO e altri

19

Rodríguez-Alvarez, M., M. Fernandez-Rivas, T. Robledo Echarren e C. Martinez-Cócera. "Persistence of Tolerance After Specific Oral Tolerance Induction". Journal of Allergy and Clinical Immunology 125, n. 2 (febbraio 2010): AB22. http://dx.doi.org/10.1016/j.jaci.2009.12.118.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

20

Kurihara, Kazuyuki. "Weaning considering oral tolerance induction". Nihon Shoni Arerugi Gakkaishi. The Japanese Journal of Pediatric Allergy and Clinical Immunology 30, n. 1 (2016): 13–20. http://dx.doi.org/10.3388/jspaci.30.13.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

21

Rezende, Rafael M., e Howard L. Weiner. "Oral tolerance: an updated review". Immunology Letters 245 (maggio 2022): 29–37. http://dx.doi.org/10.1016/j.imlet.2022.03.007.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

22

Whitacre, Caroline C. "New insights into oral tolerance". Gastroenterology 119, n. 1 (luglio 2000): 260–62. http://dx.doi.org/10.1053/gast.2000.9192.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

23

Holbrook, W. P., D. Olafsdottir, H. B. Magnusson e E. Benediktsdottir. "Penicillin tolerance among oral streptococci". Journal of Medical Microbiology 27, n. 1 (1 settembre 1988): 17–22. http://dx.doi.org/10.1099/00222615-27-1-17.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

24

Wang, Jun, e Rene EM Toes. "Mechanisms of oral tolerance revisited". Arthritis Research & Therapy 10, n. 2 (2008): 108. http://dx.doi.org/10.1186/ar2402.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

25

Ake-Uzoigwe, Rukeme, Anubha Arora, Dongping Zhang, Carolyn Salafia, Kolawole Akinnawonu e Aleksandr Fuks. "Postpartum Oral Glucose Tolerance Test". Obstetrics & Gynecology 129 (maggio 2017): 40S—41S. http://dx.doi.org/10.1097/01.aog.0000514347.83223.e8.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

26

McSorley, Stephen J., e Paul Garside. "Vaccination by inducing oral tolerance?" Immunology Today 20, n. 12 (dicembre 1999): 555–60. http://dx.doi.org/10.1016/s0167-5699(99)01539-x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

27

Meyer, Tim, Reiner Ullrich e Martin Zeitz. "Oral tolerance induction in humans". Experimental and Molecular Pathology 93, n. 3 (dicembre 2012): 449–54. http://dx.doi.org/10.1016/j.yexmp.2012.10.002.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

28

Weiner, Howard L. "Oral Tolerance: Mobilizing the Gut". Hospital Practice 30, n. 9 (15 settembre 1995): 53–58. http://dx.doi.org/10.1080/21548331.1995.11443258.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

29

DRACHMAN, DANIEL B., SEIICHI OKUMURA, ROBERT N. ADAMS e KEVIN R. McINTOSH. "Oral Tolerance in Myasthenia Gravisa". Annals of the New York Academy of Sciences 778, n. 1 (febbraio 1996): 258–72. http://dx.doi.org/10.1111/j.1749-6632.1996.tb21134.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

30

GIENAPP, INGRID, KAREN COX, NAJMA JAVED e CAROLINE WHITACRE. "Oral Tolerance in Autoimmune Encephalomyelitis." Annals of the New York Academy of Sciences 778, n. 1 (febbraio 1996): 382–83. http://dx.doi.org/10.1111/j.1749-6632.1996.tb21150.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

31

VAZ, N., A. M. C. FARIA, B. A. VERDOLIN e C. R. CARVALHO. "Immaturity, Ageing and Oral Tolerance". Scandinavian Journal of Immunology 46, n. 3 (settembre 1997): 225–29. http://dx.doi.org/10.1046/j.1365-3083.1997.d01-117.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

32

STAINES, N. A. "Oral Tolerance and Collagen Arthritis". Rheumatology 31, n. 4 (1992): 283–84. http://dx.doi.org/10.1093/rheumatology/31.4.283.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

33

Pabst, O., e A. M. Mowat. "Oral tolerance to food protein". Mucosal Immunology 5, n. 3 (8 febbraio 2012): 232–39. http://dx.doi.org/10.1038/mi.2012.4.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

34

Mayer, Lloyd, e Ling Shao. "Therapeutic potential of oral tolerance". Nature Reviews Immunology 4, n. 6 (giugno 2004): 407–19. http://dx.doi.org/10.1038/nri1370.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

35

Strobel, St, e Anne Ferguson. "Oral Tolerance - Induction and Modulation*". Klinische Pädiatrie 197, n. 04 (luglio 1985): 297–301. http://dx.doi.org/10.1055/s-2008-1033987.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

36

Telemo, Esbjörn, Malin Karlsson, Anna Dahlman-Höglund, Ulf Dahlgren e Samuel Lundin. "Oral Tolerance in Experimental Animals". International Archives of Allergy and Immunology 113, n. 1-3 (1997): 219–23. http://dx.doi.org/10.1159/000237552.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

37

Mayer, Lloyd, Kirk Sperber, Lisa Chan, Joseph Child e Lisa Toy. "Oral tolerance to protein antigens". Allergy 56, s67 (aprile 2001): 12–15. http://dx.doi.org/10.1111/j.1398-9995.2001.00904.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

38

Hohlstein, Leigh Anne, Harry E. Gwirtsman, Frank Whalen e Melvin P. Enns. "Oral glucose tolerance in bulimia". International Journal of Eating Disorders 5, n. 1 (gennaio 1986): 157–60. http://dx.doi.org/10.1002/1098-108x(198601)5:1<157::aid-eat2260050116>3.0.co;2-g.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

39

Lipkowski, A. W., B. Baranowska, E. Marczak, B. Kwiatkowska-Patzer, B. Gajkowska e M. Walski. "Protein hydrolysates for oral tolerance". BioFactors 12, n. 1-4 (2000): 147–50. http://dx.doi.org/10.1002/biof.5520120123.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

40

Wambre, Erik, e David Jeong. "Oral Tolerance Development and Maintenance". Immunology and Allergy Clinics of North America 38, n. 1 (febbraio 2018): 27–37. http://dx.doi.org/10.1016/j.iac.2017.09.003.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

41

Veldhoen, Marc. "Oral tolerance: Passing CD11b on the way to tolerance". Immunology & Cell Biology 85, n. 6 (24 luglio 2007): 397–98. http://dx.doi.org/10.1038/sj.icb.7100106.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

42

Winkelhoff, A. J., T. J. M. Steenbergen e J. Graaff. "Oxygen tolerance of oral and non-oral black-pigmentedBacteroidesspecies". FEMS Microbiology Letters 33, n. 2-3 (febbraio 1986): 215–18. http://dx.doi.org/10.1111/j.1574-6968.1986.tb01274.x.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

43

Kadono, Takafumi, Hanako Ohmatsu e Shinichi Sato. "Beta 7 integrin is essential for the induction of oral tolerance (112.15)". Journal of Immunology 186, n. 1_Supplement (1 aprile 2011): 112.15. http://dx.doi.org/10.4049/jimmunol.186.supp.112.15.

Testo completo

Abstract (sommario):

Abstract Oral tolerance is one of the hallmarks of intestinal immunity that induces systemic unresponsiveness to orally ingested antigens. Beta 7 integrin is known to mediate lymphocyte migration to gut-associated lymphoid tissues, especially Peyer’s patches. We assume that lack of beta 7 integrin might affect oral tolerance due to defective lymphocyte migration to intestinal tissues. When mice were intraperitoneally immunized with OVA following oral OVA administration, beta 7 integrin deficient mice showed defective oral tolerance measured by OVA-specific IgG and IgM antibody titers, numbers of OVA-specific antibody forming cells, and proliferative responses to OVA. Oral tolerance in L-selectin deficient mice was unimpaired. Moreover, beta 7 integrin/ L-selectin double deficient mice showed defective oral tolerance to a similar degree as beta 7 integrin deficient mice, suggesting no additive effect of L-selectin deficienty. We also measured cytokine secretion from splenocytes following oral tolerance induction and found that whereas IFN gamma secretion was decreased in wild-type mice, this reduction was abrogated in beta 7 deficient mice. These results demonstrate that beta 7 integrin is essential for oral tolerance.

Gli stili APA, Harvard, Vancouver, ISO e altri

44

Liu, Liming, Vijay K. Kuchroo e Howard L. Weiner. "B7.2 (CD86) But Not B7.1 (CD80) Costimulation Is Required for the Induction of Low Dose Oral Tolerance". Journal of Immunology 163, n. 4 (15 agosto 1999): 2284–90. http://dx.doi.org/10.4049/jimmunol.163.4.2284.

Testo completo

Abstract (sommario):

Abstract Oral administration of Ag leads to systemic unresponsiveness (oral tolerance) to the fed Ag. Oral tolerance is mediated through active suppression by Th2 or TGF-β-secreting cells or clonal anergy/deletion, depending on the Ag dose used, with low dose favoring active suppression and high dose favoring anergy/deletion. The nature of APC and inductive events leading to the generation of oral tolerance have not been well defined. To determine the role of costimulatory molecules in the induction of oral tolerance, we have tested the effect of anti-B7.1 or anti-B7.2 mAb on the induction of tolerance by both high and low dose Ag feeding regimens. Our results show that the B7.2 molecule is critical for the induction of low-dose oral tolerance. Injection of anti-B7.2 but not anti-B7.1 intact Ab or Fab fragments inhibited the oral tolerance induced by low-dose (0.5 mg) but not high-dose OVA (25 mg) feeding. In addition, anti-B7.2, but not anti-B7.1, inhibited secretion of TGF-β, one of the primary cytokines that mediates low-dose oral tolerance. Finally, in the in vivo model of experimental allergic encephalomyelitis, anti-B7.2 mAb treatment abrogated protection offered against disease by low-dose myelin basic protein feeding, while anti-B7.1 had no effect. Anti B7.2 had no effect on disease suppression by high-dose oral Ag. These data demonstrate that B7.2 costimulatory molecules play an essential role in the induction of low-dose oral tolerance.

Gli stili APA, Harvard, Vancouver, ISO e altri

45

Shakya, Akhilesh Kumar, Buddhadev Mallick e Kutty Selva Nandakumar. "A Perspective on Oral Immunotherapeutic Tools and Strategies for Autoimmune Disorders". Vaccines 11, n. 6 (27 maggio 2023): 1031. http://dx.doi.org/10.3390/vaccines11061031.

Testo completo

Abstract (sommario):

Oral immune tolerance is a physiological process to achieve tolerance against autoimmunity by oral ingestion of self-antigen(s) or other therapeutics. At the cellular level, oral tolerance suppresses autoimmune diseases by activating FoxP-positive and -negative regulatory T cells (Tregs) and/or causing clonal anergy or deletion of autoreactive T cells, affecting B cell tolerance. However, oral delivery of antigens/biologics is challenging due to their instability in the harsh environment of the gastrointestinal (GI) tract. Several antigen/drug delivery tools and approaches, including micro/nanoparticles and transgenic plant-based delivery systems, have been explored to demonstrate oral immune tolerance for different autoimmune diseases successfully. However, despite the effectiveness, variation in results, dose optimization, and undesirable immune system activation are the limitations of the oral approach to further advancement. From this perspective, the current review discusses the oral tolerance phenomenon, cellular mechanisms, antigen delivery tools and strategies, and its challenges.

Gli stili APA, Harvard, Vancouver, ISO e altri

46

Kurihara, Shunjiro, Kotaro Suzuki, Masaya Yokota, Takashi Ito, Yuki Hayashi, Ryo Kikuchi, Takahiro Kageyama et al. "Eosinophils Contribute to Oral Tolerance via Induction of RORγt-Positive Antigen-Presenting Cells and RORγt-Positive Regulatory T Cells". Biomolecules 14, n. 1 (10 gennaio 2024): 89. http://dx.doi.org/10.3390/biom14010089.

Testo completo

Abstract (sommario):

Oral tolerance has been defined as the specific suppression of immune responses to an antigen by prior oral administration of the antigen. It has been thought to serve to suppress food allergy. Previous studies have shown that dendritic cells (DCs) and regulatory T cells (Tregs) are involved in the induction of oral tolerance. However, the detailed mechanisms of Treg induction in oral tolerance remain largely unknown. Eosinophils have been recognized as effector cells in allergic diseases, but in recent years, the diverse functions of tissue-resident eosinophils have been reported. Eosinophils in the intestine have been reported to induce Tregs by releasing TGF-β, but the role of eosinophils in oral tolerance is still controversial. In this study, we analyzed the roles of eosinophils in oral tolerance using eosinophil-deficient ΔdblGATA mice (mice lacking a high-affinity GATA-binding site in the GATA1 promoter). ΔdblGATA mice showed impaired antigen-induced oral tolerance compared to wild-type mice. The induction of RORγt+ Tregs in mesenteric lymph nodes (MLNs) by oral tolerance induction was impaired in ΔdblGATA mice compared to wild-type mice. An increase in RORγt+ antigen-presenting cells (APCs), which are involved in RORγt+ Treg differentiation, in the intestine and MLNs was not seen in ΔdblGATA mice. Notably, the expansion of group 3 innate lymphoid cells (ILC3s), a subset of RORγt+ APCs, by oral tolerance induction was seen in wild-type mice but not ΔdblGATA mice. These results suggest that eosinophils are crucial in the induction of oral tolerance, possibly via the induction of RORγt+ APCs and RORγt+ Tregs.

Gli stili APA, Harvard, Vancouver, ISO e altri

47

abbas, sukardi. "Cultural Tolerance in Oral Literature Ternate". ISLLAC : Journal of Intensive Studies on Language, Literature, Art, and Culture 3, n. 1 (26 maggio 2019): 111–17. http://dx.doi.org/10.17977/um006v3i12019p111.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

48

Hachimura, Satoshi, e Shuichi Kaminogawa. "Oral tolerance and its clinical application." Japanese Journal of Clinical Immunology 22, n. 6 (1999): 466–68. http://dx.doi.org/10.2177/jsci.22.466.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

49

Pelaez-Prestel, Hector F., Jose L. Sanchez-Trincado, Esther M. Lafuente e Pedro A. Reche. "Immune Tolerance in the Oral Mucosa". International Journal of Molecular Sciences 22, n. 22 (10 novembre 2021): 12149. http://dx.doi.org/10.3390/ijms222212149.

Testo completo

Abstract (sommario):

The oral mucosa is a site of intense immune activity, where a large variety of immune cells meet to provide a first line of defense against pathogenic organisms. Interestingly, the oral mucosa is exposed to a plethora of antigens from food and commensal bacteria that must be tolerated. The mechanisms that enable this tolerance are not yet fully defined. Many works have focused on active immune mechanisms involving dendritic and regulatory T cells. However, epithelial cells also make a major contribution to tolerance by influencing both innate and adaptive immunity. Therefore, the tolerogenic mechanisms concurring in the oral mucosa are intertwined. Here, we review them systematically, paying special attention to the role of oral epithelial cells.

Gli stili APA, Harvard, Vancouver, ISO e altri

50

MOWAT, ALLAN McI, LUCY A. PARKER, HELEN BEACOCK-SHARP, Owain R. Millington e FERNANDO CHIRDO. "Oral Tolerance: Overview and Historical Perspectives". Annals of the New York Academy of Sciences 1029, n. 1 (dicembre 2004): 1–8. http://dx.doi.org/10.1196/annals.1309.001.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

Articoli di riviste sul tema "Oral tolerance"

Cita una fonte nei formati APA, MLA, Chicago, Harvard e in molti altri stili