Helminth-derived proteins as immune system regulators: a systematic review of their promise in alleviating colitis

Helminth-derived proteins have immunomodulatory properties, influencing the host’s immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately fa...

Full description

Saved in:
Bibliographic Details
Published inBMC immunology Vol. 25; no. 1; pp. 21 - 10
Main Authors Alghanmi, Maimonah, Minshawi, Faisal, Altorki, Tarfa A., Zawawi, Ayat, Alsaady, Isra, Naser, Abdallah Y, Alwafi, Hassan, Alsulami, Soa’ad M., Azhari, Ala A., Hashem, Anwar M, Alhabbab, Rowa
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 18.04.2024
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Helminth-derived proteins have immunomodulatory properties, influencing the host’s immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately favouring a Th2-biased immune response. This systematic review focused on helminth-derived proteins and explored their impact on reducing inflammatory responses in mouse models of colitis. A systematic search across Medline, EMBASE, Web of Science, and Cochrane Library identified fourteen relevant studies. These studies reported immunomodulatory changes, including increased production of anti-inflammatory cells and cytokines. In mouse models of colitis treated with on helminth-derived proteins, significant improvements in pathological parameters such as body weight, colon length, and microscopic inflammatory scores were observed compared to control groups. Moreover, helminth-derived proteins can enhance the function of Tregs and alleviate the severity of inflammatory conditions. The findings underscore the pivotal role of helminth-derived proteins in immunomodulation, specifically in the axis of cytokine secretion and immune cell polarization. The findings offer new opportunities for treating chronic inflammatory conditions such Crohn’s disease.
AbstractList Helminth-derived proteins have immunomodulatory properties, influencing the host's immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately favouring a Th2-biased immune response. This systematic review focused on helminth-derived proteins and explored their impact on reducing inflammatory responses in mouse models of colitis. A systematic search across Medline, EMBASE, Web of Science, and Cochrane Library identified fourteen relevant studies. These studies reported immunomodulatory changes, including increased production of anti-inflammatory cells and cytokines. In mouse models of colitis treated with on helminth-derived proteins, significant improvements in pathological parameters such as body weight, colon length, and microscopic inflammatory scores were observed compared to control groups. Moreover, helminth-derived proteins can enhance the function of Tregs and alleviate the severity of inflammatory conditions. The findings underscore the pivotal role of helminth-derived proteins in immunomodulation, specifically in the axis of cytokine secretion and immune cell polarization. The findings offer new opportunities for treating chronic inflammatory conditions such Crohn's disease. Keywords: Helminths, Immunoregulation, Inflammatory bowel disease, Colitis, Ulcerative colitis, Crohn's disease
Helminth-derived proteins have immunomodulatory properties, influencing the host's immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately favouring a Th2-biased immune response. This systematic review focused on helminth-derived proteins and explored their impact on reducing inflammatory responses in mouse models of colitis. A systematic search across Medline, EMBASE, Web of Science, and Cochrane Library identified fourteen relevant studies. These studies reported immunomodulatory changes, including increased production of anti-inflammatory cells and cytokines. In mouse models of colitis treated with on helminth-derived proteins, significant improvements in pathological parameters such as body weight, colon length, and microscopic inflammatory scores were observed compared to control groups. Moreover, helminth-derived proteins can enhance the function of Tregs and alleviate the severity of inflammatory conditions. The findings underscore the pivotal role of helminth-derived proteins in immunomodulation, specifically in the axis of cytokine secretion and immune cell polarization. The findings offer new opportunities for treating chronic inflammatory conditions such Crohn's disease.Helminth-derived proteins have immunomodulatory properties, influencing the host's immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately favouring a Th2-biased immune response. This systematic review focused on helminth-derived proteins and explored their impact on reducing inflammatory responses in mouse models of colitis. A systematic search across Medline, EMBASE, Web of Science, and Cochrane Library identified fourteen relevant studies. These studies reported immunomodulatory changes, including increased production of anti-inflammatory cells and cytokines. In mouse models of colitis treated with on helminth-derived proteins, significant improvements in pathological parameters such as body weight, colon length, and microscopic inflammatory scores were observed compared to control groups. Moreover, helminth-derived proteins can enhance the function of Tregs and alleviate the severity of inflammatory conditions. The findings underscore the pivotal role of helminth-derived proteins in immunomodulation, specifically in the axis of cytokine secretion and immune cell polarization. The findings offer new opportunities for treating chronic inflammatory conditions such Crohn's disease.
Helminth-derived proteins have immunomodulatory properties, influencing the host's immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately favouring a Th2-biased immune response. This systematic review focused on helminth-derived proteins and explored their impact on reducing inflammatory responses in mouse models of colitis. A systematic search across Medline, EMBASE, Web of Science, and Cochrane Library identified fourteen relevant studies. These studies reported immunomodulatory changes, including increased production of anti-inflammatory cells and cytokines. In mouse models of colitis treated with on helminth-derived proteins, significant improvements in pathological parameters such as body weight, colon length, and microscopic inflammatory scores were observed compared to control groups. Moreover, helminth-derived proteins can enhance the function of Tregs and alleviate the severity of inflammatory conditions. The findings underscore the pivotal role of helminth-derived proteins in immunomodulation, specifically in the axis of cytokine secretion and immune cell polarization. The findings offer new opportunities for treating chronic inflammatory conditions such Crohn's disease.
Abstract Helminth-derived proteins have immunomodulatory properties, influencing the host’s immune response as an adaptive strategy for helminth survival. Helminth-derived proteins modulate the immune response by inducing anti-inflammatory cytokines, promoting regulatory T-cell development, and ultimately favouring a Th2-biased immune response. This systematic review focused on helminth-derived proteins and explored their impact on reducing inflammatory responses in mouse models of colitis. A systematic search across Medline, EMBASE, Web of Science, and Cochrane Library identified fourteen relevant studies. These studies reported immunomodulatory changes, including increased production of anti-inflammatory cells and cytokines. In mouse models of colitis treated with on helminth-derived proteins, significant improvements in pathological parameters such as body weight, colon length, and microscopic inflammatory scores were observed compared to control groups. Moreover, helminth-derived proteins can enhance the function of Tregs and alleviate the severity of inflammatory conditions. The findings underscore the pivotal role of helminth-derived proteins in immunomodulation, specifically in the axis of cytokine secretion and immune cell polarization. The findings offer new opportunities for treating chronic inflammatory conditions such Crohn’s disease.
ArticleNumber 21
Audience Academic
Author Alghanmi, Maimonah
Minshawi, Faisal
Azhari, Ala A.
Naser, Abdallah Y
Altorki, Tarfa A.
Zawawi, Ayat
Alsaady, Isra
Alsulami, Soa’ad M.
Hashem, Anwar M
Alhabbab, Rowa
Alwafi, Hassan
Author_xml – sequence: 1
  givenname: Maimonah
  surname: Alghanmi
  fullname: Alghanmi, Maimonah
– sequence: 2
  givenname: Faisal
  surname: Minshawi
  fullname: Minshawi, Faisal
– sequence: 3
  givenname: Tarfa A.
  surname: Altorki
  fullname: Altorki, Tarfa A.
– sequence: 4
  givenname: Ayat
  surname: Zawawi
  fullname: Zawawi, Ayat
– sequence: 5
  givenname: Isra
  surname: Alsaady
  fullname: Alsaady, Isra
– sequence: 6
  givenname: Abdallah Y
  surname: Naser
  fullname: Naser, Abdallah Y
– sequence: 7
  givenname: Hassan
  surname: Alwafi
  fullname: Alwafi, Hassan
– sequence: 8
  givenname: Soa’ad M.
  surname: Alsulami
  fullname: Alsulami, Soa’ad M.
– sequence: 9
  givenname: Ala A.
  surname: Azhari
  fullname: Azhari, Ala A.
– sequence: 10
  givenname: Anwar M
  surname: Hashem
  fullname: Hashem, Anwar M
– sequence: 11
  givenname: Rowa
  surname: Alhabbab
  fullname: Alhabbab, Rowa
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38637733$$D View this record in MEDLINE/PubMed
BookMark eNp9kktv1DAUhSNURB_wB1igSGxgkeJXYg8bVFVAR6qExGNtOc51xqPEHmxnoP8epzNUMxVCWSS69zsn8ck5L06cd1AULzG6xFg07yImoqkrRFiFUINZRZ4UZ5hxXBHMycnB82lxHuMaIcwFEc-KUyoayjmlZ0W4gWG0Lq2qDoLdQldugk9gXSxVLO04Tg7KeBcTjGWAfhpU8iG-L9V-qJLVebG18Kv0pkwrsGG2GG2E0rpSDUNeZsr1pfaDTTY-L54aNUR4sb9fFD8-ffx-fVPdfvm8vL66rXS9EKkyiEJXs7ojLUdcaCFMyzFQLQwwyOdVotHE8LoTyiw0R7BAtENUMMpQp4FeFMudb-fVWm6CHVW4k15ZeT_woZcq5M8fQHZGY8yoRvUCmGFKLVhLiG4brlqGGMteH3Zem6kdIbu7FNRwZHq8cXYle7-VGCNSk5pnhzd7h-B_ThCTzBFpGAblwE9RUsQo4vln0Yy-foSu_RRczipTNcO84eSA6lU-gXXG5xfr2VRe8cVshfBMXf6DylcHo9W5T8bm-ZHg7ZEgMwl-p15NMcrlt6_H7KvDVB7i-FuvDJAdoIOPMYB5QDCSc4flrsMyd1jed1iSLBKPRNqm3CA_J2uH_0n_AOY99Rs
CitedBy_id crossref_primary_10_3390_pathogens14030223
crossref_primary_10_1186_s12865_024_00661_9
crossref_primary_10_2147_JIR_S493374
crossref_primary_10_3390_v17030451
Cites_doi 10.1128/IAI.00851-18
10.1007/s11010-011-1046-4
10.1111/j.0105-2896.2004.00191.x
10.3390/pathogens5030058
10.1016/j.cellimm.2015.10.006
10.1146/annurev-immunol-030409-101225
10.1016/j.jbc.2021.100834
10.1186/1471-2288-14-43
10.1016/j.exppara.2021.108189
10.1111/pim.12175
10.3389/fmicb.2017.02164
10.1152/ajpgi.90462.2008
10.1177/1352458514568173
10.1038/ng1096-181
10.1371/journal.pone.0209681
10.1371/journal.pntd.0001516
10.1186/s13071-015-1288-1
10.1038/cti.2017.42
10.1001/jama.283.15.2008
10.1053/gast.2002.1231527
10.1177/1352458517736377
10.1016/j.actatropica.2020.105553
10.1001/archsurg.1985.01390300013002
10.1111/j.1440-1681.2006.04400.x
10.1371/journal.pone.0110002
10.1016/S0020-7519(03)00175-9
10.1007/s12016-014-8458-3
10.1007/s00436-017-5544-5
10.1111/cei.13199
10.1128/CMR.14.4.689-703.2001
10.1128/IAI.01156-06
10.1016/S0960-9822(01)00118-X
10.1074/jbc.M109.060368
10.4049/jimmunol.1401217
10.1038/nprot.2007.41
10.7150/thno.20359
10.3389/fcell.2021.695015
10.1084/jem.182.5.1579
10.1002/ibd.20787
10.1016/S0020-7519(03)00163-2
10.1111/1751-2980.12290
10.1017/S0031182008005210
10.1186/1471-2172-10-9
10.1007/s10620-011-1689-8
10.3347/kjp.2011.49.3.245
10.1128/IAI.00563-12
10.1007/s12291-017-0671-4
10.1038/mi.2015.62
10.1084/jem.20111381
10.1016/j.trsl.2021.02.012
10.1016/j.ijpara.2016.07.008
10.1136/bmj.b2535
10.4049/jimmunol.2000290
10.1002/ibd.21629
10.1038/sj.cdd.4401850
10.1111/pim.12425
10.1111/j.1600-065X.2009.00799.x
10.1128/IAI.71.5.2422-2429.2003
10.1371/journal.pone.0055487
10.1016/j.jaci.2016.07.007
ContentType Journal Article
Copyright 2024. The Author(s).
COPYRIGHT 2024 BioMed Central Ltd.
2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
The Author(s) 2024
Copyright_xml – notice: 2024. The Author(s).
– notice: COPYRIGHT 2024 BioMed Central Ltd.
– notice: 2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: The Author(s) 2024
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
ISR
3V.
7T5
7X7
7XB
88E
8C1
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
H94
HCIFZ
K9.
LK8
M0S
M1P
M7P
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1186/s12865-024-00614-2
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Gale In Context: Science
ProQuest Central (Corporate)
Immunology Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Public Health Database
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni Edition)
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
AIDS and Cancer Research Abstracts
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
Health & Medical Collection (Alumni Edition)
Medical Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Biological Science Collection
AIDS and Cancer Research Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Public Health
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Immunology Abstracts
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
MEDLINE
Publicly Available Content Database



CrossRef

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Biology
EISSN 1471-2172
EndPage 10
ExternalDocumentID oai_doaj_org_article_dfc1143c059e4f4aa94b22cb67ab4044
PMC11025257
A790721013
38637733
10_1186_s12865_024_00614_2
Genre Research Support, Non-U.S. Gov't
Systematic Review
Journal Article
GeographicLocations Saudi Arabia
GeographicLocations_xml – name: Saudi Arabia
GrantInformation_xml – fundername: the Ministry of Education and King Abdulaziz University, Jeddah, Saudi Arabia
  grantid: IFPRC-408160-290-2020
GroupedDBID ---
0R~
23N
2WC
53G
5VS
6J9
7X7
88E
8C1
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACMJI
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AENEX
AFKRA
AFPKN
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BBNVY
BCNDV
BENPR
BFQNJ
BHPHI
BMC
BPHCQ
C6C
CCPQU
CITATION
CS3
DIK
DU5
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HMCUK
HYE
IAO
IHR
INH
INR
ISR
ITC
KQ8
LGEZI
LOTEE
M1P
M48
M7P
M~E
NADUK
NXXTH
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SBL
SOJ
SV3
TR2
TUS
UKHRP
W2D
WOQ
WOW
XSB
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
PQGLB
PMFND
3V.
7T5
7XB
8FE
8FH
8FK
AZQEC
DWQXO
GNUQQ
H94
K9.
LK8
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c598t-f03ed545d2b7078c88fb71e3c8fe4e061a86c2f75d8af9c70e903d0384340dce3
IEDL.DBID DOA
ISSN 1471-2172
IngestDate Wed Aug 27 01:20:54 EDT 2025
Thu Aug 21 18:34:08 EDT 2025
Fri Jul 11 15:34:09 EDT 2025
Fri Jul 25 19:24:30 EDT 2025
Tue Jun 17 22:14:46 EDT 2025
Tue Jun 10 21:10:33 EDT 2025
Fri Jun 27 05:52:30 EDT 2025
Tue Aug 19 01:31:00 EDT 2025
Tue Jul 01 03:29:40 EDT 2025
Thu Apr 24 23:00:13 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Inflammatory bowel disease
Colitis
Immunoregulation
Helminths
Crohn’s disease
Ulcerative colitis
Language English
License 2024. The Author(s).
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c598t-f03ed545d2b7078c88fb71e3c8fe4e061a86c2f75d8af9c70e903d0384340dce3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Undefined-1
ObjectType-Feature-3
content type line 23
OpenAccessLink https://doaj.org/article/dfc1143c059e4f4aa94b22cb67ab4044
PMID 38637733
PQID 3054176723
PQPubID 44823
PageCount 10
ParticipantIDs doaj_primary_oai_doaj_org_article_dfc1143c059e4f4aa94b22cb67ab4044
pubmedcentral_primary_oai_pubmedcentral_nih_gov_11025257
proquest_miscellaneous_3043072173
proquest_journals_3054176723
gale_infotracmisc_A790721013
gale_infotracacademiconefile_A790721013
gale_incontextgauss_ISR_A790721013
pubmed_primary_38637733
crossref_primary_10_1186_s12865_024_00614_2
crossref_citationtrail_10_1186_s12865_024_00614_2
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-04-18
PublicationDateYYYYMMDD 2024-04-18
PublicationDate_xml – month: 04
  year: 2024
  text: 2024-04-18
  day: 18
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle BMC immunology
PublicationTitleAlternate BMC Immunol
PublicationYear 2024
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References 614_CR34
JK Nono (614_CR46) 2012; 6
X Bai (614_CR50) 2012; 360
RM Maizels (614_CR5) 2016; 138
Z Wu (614_CR9) 2017; 8
V Khatri (614_CR22) 2015; 16
P Wangchuk (614_CR39) 2019; 87
E van Riet (614_CR48) 2009; 10
DA Harn (614_CR47) 2009; 230
S Hartmann (614_CR56) 2003; 33
NA Hosken (614_CR61) 1995; 182
T Arai (614_CR15) 2022; 232
D Moher (614_CR20) 2009; 339
P Schierack (614_CR53) 2003; 71
W Liu (614_CR60) 2013; 8
N Xu (614_CR59) 2021; 206
M Heylen (614_CR37) 2014; 9
D Cooper (614_CR55) 2016; 5
T Kawai (614_CR45) 2006; 13
T Ziegler (614_CR58) 2015; 194
MJG Johnston (614_CR7) 2009; 136
L Wang (614_CR25) 2017; 7
CJC Johnston (614_CR62) 2016; 299
S Marquet (614_CR2) 1996; 14
614_CR29
614_CR27
A Voldsgaard (614_CR17) 2015; 21
V Driss (614_CR24) 2016; 9
B Everts (614_CR52) 2012; 209
G Buitrago (614_CR28) 2021; 232
L Du (614_CR31) 2011; 56
RM Maizels (614_CR3) 2004; 201
A Sarazin (614_CR26) 2018; 13
NE Ruyssers (614_CR38) 2009; 15
GGL Cancado (614_CR42) 2011; 17
A Kaser (614_CR10) 2010; 28
SW Jang (614_CR35) 2011; 49
Z Qu (614_CR32) 2020; 211
614_CR13
I Ferreira (614_CR41) 2013; 81
S Coronado (614_CR30) 2017; 39
JO Fleming (614_CR36) 2015; 37
S Donnelly (614_CR51) 2010; 285
J Cvetkovic (614_CR49) 2016; 46
614_CR19
DV Ostanin (614_CR12) 2009; 296
W Harnett (614_CR4) 2006; 33
R Riganò (614_CR44) 2007; 75
J Schölmerich (614_CR18) 2017; 11
TB Smallwood (614_CR40) 2021; 297
CR Hooijmans (614_CR21) 2014; 14
JV Weinstock (614_CR6) 2015; 49
J Fleming (614_CR16) 2019; 25
PE Donahue (614_CR54) 1985; 120
B Manoury (614_CR57) 2001; 11
614_CR43
S Wirtz (614_CR14) 2007; 2
M Wang (614_CR8) 2017; 116
RJ Quinnell (614_CR1) 2003; 33
NS Togre (614_CR23) 2018; 33
DJ Berg (614_CR11) 2002; 123
J Xu (614_CR33) 2018; 194
39367320 - BMC Immunol. 2024 Oct 4;25(1):65. doi: 10.1186/s12865-024-00661-9.
References_xml – volume: 11
  start-page: 390
  year: 2017
  ident: 614_CR18
  publication-title: J Crohns Colitis
– volume: 87
  start-page: 4
  year: 2019
  ident: 614_CR39
  publication-title: Infect Immun
  doi: 10.1128/IAI.00851-18
– volume: 360
  start-page: 79
  year: 2012
  ident: 614_CR50
  publication-title: Mol Cell Biochem
  doi: 10.1007/s11010-011-1046-4
– volume: 201
  start-page: 89
  year: 2004
  ident: 614_CR3
  publication-title: Immunol Rev
  doi: 10.1111/j.0105-2896.2004.00191.x
– volume: 5
  start-page: 58
  year: 2016
  ident: 614_CR55
  publication-title: Pathogens
  doi: 10.3390/pathogens5030058
– volume: 299
  start-page: 14
  year: 2016
  ident: 614_CR62
  publication-title: Cell Immunol
  doi: 10.1016/j.cellimm.2015.10.006
– volume: 28
  start-page: 573
  year: 2010
  ident: 614_CR10
  publication-title: Annu Rev Immunol
  doi: 10.1146/annurev-immunol-030409-101225
– volume: 297
  start-page: 100834
  year: 2021
  ident: 614_CR40
  publication-title: J Biol Chem
  doi: 10.1016/j.jbc.2021.100834
– volume: 14
  start-page: 43
  year: 2014
  ident: 614_CR21
  publication-title: BMC Med Res Methodol
  doi: 10.1186/1471-2288-14-43
– volume: 232
  start-page: 108189
  year: 2022
  ident: 614_CR15
  publication-title: Exp Parasitol
  doi: 10.1016/j.exppara.2021.108189
– volume: 37
  start-page: 277
  year: 2015
  ident: 614_CR36
  publication-title: Parasite Immunol
  doi: 10.1111/pim.12175
– volume: 8
  start-page: 2164
  year: 2017
  ident: 614_CR9
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2017.02164
– volume: 296
  start-page: G135
  year: 2009
  ident: 614_CR12
  publication-title: Am J Physiology-Gastrointestinal Liver Physiol
  doi: 10.1152/ajpgi.90462.2008
– volume: 21
  start-page: 1723
  year: 2015
  ident: 614_CR17
  publication-title: Mult Scler
  doi: 10.1177/1352458514568173
– volume: 14
  start-page: 181
  year: 1996
  ident: 614_CR2
  publication-title: Nat Genet
  doi: 10.1038/ng1096-181
– volume: 13
  start-page: e0209681
  year: 2018
  ident: 614_CR26
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0209681
– volume: 6
  start-page: e1516
  year: 2012
  ident: 614_CR46
  publication-title: PLoS Negl Trop Dis
  doi: 10.1371/journal.pntd.0001516
– ident: 614_CR13
  doi: 10.1186/s13071-015-1288-1
– ident: 614_CR27
  doi: 10.1038/cti.2017.42
– ident: 614_CR19
  doi: 10.1001/jama.283.15.2008
– volume: 123
  start-page: 1527
  year: 2002
  ident: 614_CR11
  publication-title: Gastroenterology
  doi: 10.1053/gast.2002.1231527
– volume: 25
  start-page: 81
  year: 2019
  ident: 614_CR16
  publication-title: Mult Scler
  doi: 10.1177/1352458517736377
– volume: 211
  start-page: 105553
  year: 2020
  ident: 614_CR32
  publication-title: Acta Trop
  doi: 10.1016/j.actatropica.2020.105553
– volume: 120
  start-page: 663
  year: 1985
  ident: 614_CR54
  publication-title: Arch Surg
  doi: 10.1001/archsurg.1985.01390300013002
– volume: 33
  start-page: 511
  year: 2006
  ident: 614_CR4
  publication-title: Clin Exp Pharmacol Physiol
  doi: 10.1111/j.1440-1681.2006.04400.x
– volume: 9
  start-page: e110002
  year: 2014
  ident: 614_CR37
  publication-title: PLoS ONE [Electronic Resource]
  doi: 10.1371/journal.pone.0110002
– volume: 33
  start-page: 1219
  year: 2003
  ident: 614_CR1
  publication-title: Int J Parasitol
  doi: 10.1016/S0020-7519(03)00175-9
– volume: 49
  start-page: 227
  year: 2015
  ident: 614_CR6
  publication-title: Clin Rev Allergy Immunol
  doi: 10.1007/s12016-014-8458-3
– volume: 116
  start-page: 2065
  year: 2017
  ident: 614_CR8
  publication-title: Parasitol Res
  doi: 10.1007/s00436-017-5544-5
– volume: 194
  start-page: 400
  year: 2018
  ident: 614_CR33
  publication-title: Clin Exp Immunol
  doi: 10.1111/cei.13199
– ident: 614_CR43
  doi: 10.1128/CMR.14.4.689-703.2001
– volume: 75
  start-page: 1667
  year: 2007
  ident: 614_CR44
  publication-title: Infect Immun
  doi: 10.1128/IAI.01156-06
– ident: 614_CR29
  doi: 10.1016/j.jbc.2021.100834
– volume: 11
  start-page: 447
  year: 2001
  ident: 614_CR57
  publication-title: Curr Biol
  doi: 10.1016/S0960-9822(01)00118-X
– volume: 285
  start-page: 3383
  year: 2010
  ident: 614_CR51
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M109.060368
– volume: 194
  start-page: 1555
  year: 2015
  ident: 614_CR58
  publication-title: J Immunol
  doi: 10.4049/jimmunol.1401217
– volume: 2
  start-page: 541
  year: 2007
  ident: 614_CR14
  publication-title: Nat Protoc
  doi: 10.1038/nprot.2007.41
– volume: 7
  start-page: 3446
  year: 2017
  ident: 614_CR25
  publication-title: Theranostics
  doi: 10.7150/thno.20359
– ident: 614_CR34
  doi: 10.3389/fcell.2021.695015
– volume: 182
  start-page: 1579
  year: 1995
  ident: 614_CR61
  publication-title: J Exp Med
  doi: 10.1084/jem.182.5.1579
– volume: 15
  start-page: 491
  year: 2009
  ident: 614_CR38
  publication-title: Inflamm Bowel Dis
  doi: 10.1002/ibd.20787
– volume: 33
  start-page: 1291
  year: 2003
  ident: 614_CR56
  publication-title: Int J Parasitol
  doi: 10.1016/S0020-7519(03)00163-2
– volume: 16
  start-page: 585
  year: 2015
  ident: 614_CR22
  publication-title: J Dig Dis
  doi: 10.1111/1751-2980.12290
– volume: 136
  start-page: 125
  year: 2009
  ident: 614_CR7
  publication-title: Parasitology
  doi: 10.1017/S0031182008005210
– volume: 10
  start-page: 9
  year: 2009
  ident: 614_CR48
  publication-title: BMC Immunol
  doi: 10.1186/1471-2172-10-9
– volume: 56
  start-page: 2810
  year: 2011
  ident: 614_CR31
  publication-title: Dig Dis Sci
  doi: 10.1007/s10620-011-1689-8
– volume: 49
  start-page: 245
  year: 2011
  ident: 614_CR35
  publication-title: Korean J Parasitol
  doi: 10.3347/kjp.2011.49.3.245
– volume: 81
  start-page: 2104
  issue: 6
  year: 2013
  ident: 614_CR41
  publication-title: Infect Immun
  doi: 10.1128/IAI.00563-12
– volume: 33
  start-page: 282
  year: 2018
  ident: 614_CR23
  publication-title: Indian J Clin Biochem
  doi: 10.1007/s12291-017-0671-4
– volume: 9
  start-page: 322
  year: 2016
  ident: 614_CR24
  publication-title: Mucosal Immunol
  doi: 10.1038/mi.2015.62
– volume: 209
  start-page: 1753
  year: 2012
  ident: 614_CR52
  publication-title: J Exp Med
  doi: 10.1084/jem.20111381
– volume: 232
  start-page: 88
  year: 2021
  ident: 614_CR28
  publication-title: Transl Res
  doi: 10.1016/j.trsl.2021.02.012
– volume: 46
  start-page: 833
  year: 2016
  ident: 614_CR49
  publication-title: Int J Parasitol
  doi: 10.1016/j.ijpara.2016.07.008
– volume: 339
  start-page: b2535
  issue: jul21 1
  year: 2009
  ident: 614_CR20
  publication-title: BMJ
  doi: 10.1136/bmj.b2535
– volume: 206
  start-page: 963
  year: 2021
  ident: 614_CR59
  publication-title: J Immunol
  doi: 10.4049/jimmunol.2000290
– volume: 17
  start-page: 2275
  year: 2011
  ident: 614_CR42
  publication-title: Inflamm Bowel Dis
  doi: 10.1002/ibd.21629
– volume: 13
  start-page: 816
  year: 2006
  ident: 614_CR45
  publication-title: Cell Death Differ
  doi: 10.1038/sj.cdd.4401850
– volume: 39
  start-page: 4
  year: 2017
  ident: 614_CR30
  publication-title: Parasite Immunol
  doi: 10.1111/pim.12425
– volume: 230
  start-page: 247
  year: 2009
  ident: 614_CR47
  publication-title: Immunol Rev
  doi: 10.1111/j.1600-065X.2009.00799.x
– volume: 71
  start-page: 2422
  year: 2003
  ident: 614_CR53
  publication-title: Infect Immun
  doi: 10.1128/IAI.71.5.2422-2429.2003
– volume: 8
  start-page: e55487
  year: 2013
  ident: 614_CR60
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0055487
– volume: 138
  start-page: 666
  year: 2016
  ident: 614_CR5
  publication-title: J Allergy Clin Immunol
  doi: 10.1016/j.jaci.2016.07.007
– reference: 39367320 - BMC Immunol. 2024 Oct 4;25(1):65. doi: 10.1186/s12865-024-00661-9.
SSID ssj0017828
Score 2.3974483
SecondaryResourceType review_article
Snippet Helminth-derived proteins have immunomodulatory properties, influencing the host’s immune response as an adaptive strategy for helminth survival....
Helminth-derived proteins have immunomodulatory properties, influencing the host's immune response as an adaptive strategy for helminth survival....
Abstract Helminth-derived proteins have immunomodulatory properties, influencing the host’s immune response as an adaptive strategy for helminth survival....
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 21
SubjectTerms Analysis
Animal models
Animals
Anti-inflammatory drugs
Bacterial infections
Body mass index
Body weight
Care and treatment
Clinical outcomes
Clinical trials
Colitis
Colitis - therapy
Complications and side effects
Crohn's disease
Cytokines
Cytokines - metabolism
Diagnosis
Disease Models, Animal
Genetic engineering
Health aspects
Helminth Proteins - therapeutic use
Helminthiasis
Helminths
Immune response
Immune system
Immune System - metabolism
Immunologic Factors
Immunomodulation
Immunoregulation
Infections
Inflammation
Inflammatory bowel disease
Inflammatory bowel diseases
Laboratory animals
Lymphocytes T
Mice
Multiple sclerosis
Nematodes
Parasites
Proteins
Systematic review
T cells
Tropical diseases
Tumor necrosis factor-TNF
Ulcerative colitis
SummonAdditionalLinks – databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3daxQxEA9aUXwRrV-nVaIIPkjoZpPdZH2RKpYq1Ae10LeQZJPrge7W27uC_70z2dy1i9C3JZkNuzOTzCSZ-Q0hb8DmOl9pz6K0NZPSceY4PFVK6uiVrouI2cjH3-qjE_n1tDrNB25DDqvcrIlpoW57j2fk-6CXkqtaleLD-R-GVaPwdjWX0LhJbiF0GYZ0qdPthouD9dObRBld7w8c0zAZWCWGlluycmKMEmb__yvzFdM0DZu8YocO75N72YGkB6PEH5Abodslt8eSkn93yZ3jfFn-kCzBpPxedKsz1oKaXYSWJlCGRTdQO9AFJoYEOiI50-VYkr5fDu-ppZfwznRMbaF9pOlKAYcAzQh00VGswnKBku3m1KcwuuEROTn8_PPTEcslFpivGr1isRChBSeqLR3C_nito1M8CK9jkAGYZHXty6iqVtvYeFWEphBtIbQUsgBGiMdkp-u78JTQpnLQ7pzmAnwsC_Oc82iLyEPTSCftjPANr43P-ONYBuOXSfsQXZtRPgbkY5J8TDkj77bvnI_oG9dSf0QRbikROTs19Mu5yRPRtNHDFlB4cCuDBAW18HFl6V2trJOFlDPyGhXAIDZGh8E3c7seBvPlx3dzoBpEkwOneUbeZqLYwz94m3MZgBMIpzWh3JtQgoj8tHujZyYvHoO5VPUZebXtxjcxIK4L_RpppMAxFNA8GdVy-99C10IpAT16orATxkx7usVZghYHZ7BEfNxn13_Xc3K3TNNIMq73yM5quQ4vwDlbuZdpBv4DJNo36Q
  priority: 102
  providerName: ProQuest
– databaseName: Scholars Portal Journals: Open Access
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3di9QwEA_HieKL6Plxq6dEEXyQaNukTSqInOJxCuuDunBvIUmTvYWzvWt3D--_dybt7l3x8Mm30pmUZj4yE5L5DSEvIeZalyvHgjAFE8KmzKbwlEuhgpOqSAJWI0-_FYcz8fUoP9oi63ZHgwC7a7d22E9q1p68-X128QEc_n10eFW87VIsr2QQbRhGZMFgSb4BkUmio07F5akCREO1Lpy5dtwoOEUM_79X6iuhanyN8kpcOrhL7gwJJd3vLeAe2fL1DrnZt5i82CG3psPh-X3SQoj5taiXx6wCszv3FY0gDYu6o6ajCywU8bRHdqZt36K-abt31NBLuGfal7rQJtB4xICfAEvxdFFT7Mpyjpqu59TFa3XdAzI7-Pzz0yEbWi4wl5dqyULCfQVJVZVZhAFySgUrU8-dCl54EJJRhcuCzCtlQulk4suEVwlXgosEBMEfku26qf0uoWVu4b21KuWQcxnw-zQNJgmpL0thhZmQdC1r7QY8cmyLcaLjvkQVutePBv3oqB-dTcjrzZjTHo3jn9wfUYUbTkTSji-adq4Hx9RVcLAl5A7STC_AYA38XJY5W0hjRSLEhLxAA9CIlVHjZZy5WXWd_vLju96XJaLLQRI9Ia8GptDAHJwZahtAEgivNeLcG3GCityYvLYzvfYFDUsyGHMhMyA_35BxJF6Qq32zQh7B8RsSeB71ZrmZN1cFl5IDRY0MdiSYMaVeHEeocUgOM8TLffw_RPmE3M6iswmWqj2yvWxX_imkdEv7LPrpH8bASEA
  priority: 102
  providerName: Scholars Portal
Title Helminth-derived proteins as immune system regulators: a systematic review of their promise in alleviating colitis
URI https://www.ncbi.nlm.nih.gov/pubmed/38637733
https://www.proquest.com/docview/3054176723
https://www.proquest.com/docview/3043072173
https://pubmed.ncbi.nlm.nih.gov/PMC11025257
https://doaj.org/article/dfc1143c059e4f4aa94b22cb67ab4044
Volume 25
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3daxQxEA9aUfoiWr9O6xFF8EFCN5vsJutbW1qqcEWqhXsLSTZpD3Sv3N4V_O-dye6dtwj64suy7MyG3ZlJZkJmfkPIO_C5zhfasyhtyaR0nDkOd4WSOnqlyyxiNfLkvDy7lJ-nxXSr1RfmhHXwwJ3gDuroIWQXHsKAIGFAW0mX596VyjqZyYQECj5vvZnqzw_A7-l1iYwuD1qOBZgM_BFDny1ZPnBDCa3_zzV5yykNEya3PNDpI_KwDx3pYffJj8md0OyR-10zyZ975MGkPyZ_QhbgTH7MmuU1q8HAbkNNExzDrGmpbekMS0IC7TCc6aJrRj9ftB-ppb-BnWlX1ELnkabDBBwCbCLQWUOx_8ot6rS5oj4l0LVPyeXpybfjM9Y3V2C-qPSSxUyEGsKnOncI-OO1jk7xILyOQQYQktWlz6Mqam1j5VUWqkzUmdBSyAwEIZ6RnWbehBeEVoWD585pLiC6sjDDOY82izxUoCxpR4SvZW18jzyODTC-m7QD0aXp9GNAPybpx-Qj8mHzzk2Hu_FX7iNU4YYTMbPTA7Ak01uS-ZcljchbNACDqBgNpt1c2VXbmk9fL8yhqhBHDsLlEXnfM8U5_IO3fRUDSAKBtAac-wNOUJEfktd2ZvplozWw-EquSpUD-c2GjG9iKlwT5ivkkQLHUMDzvDPLzX8LXQqlBFD0wGAHghlSmtl1AhWHMDBHZNyX_0OUr8huniabZFzvk53lYhVeQ_C2dGNyV00VXPUxH5N7RyfnXy7Gae7CdSL1L_F5ROo
linkProvider Directory of Open Access Journals
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKEY8LgvJaKGAQiEMVNY6d2EFCqDyqXdrtAVppb8Zx7O1KkJTNblH_FL-RmTy2jZB66y2KJ1bimfE3jj3fEPIaMDezsbKBFyYJhMhYkDG4iqVQ3kqVhB6zkccHyfBIfJ3EkzXyt8uFwWOV3ZxYT9R5afEf-TbYpWAykRH_cPI7wKpRuLvaldBozGLPnf2BJVv1fvQZ9Psmina_HH4aBm1VgcDGqVoEPuQuh7ghjzJkurFK-Uwyx63yTjiAN6MSG3kZ58r41MrQpSHPQ64EF2FuHYd-r5HrALwhepScrBZ4DNBWdYk5KtmuGKZ9BoCCAUYKIoh64FfXCPgfCS5AYf-Y5gXc271L7rQBK91pLOweWXPFBrnRlLA82yA3x-3m_H0yBwj7NSsWx0EOZn3qclqTQMyKipqKzjARxdGGOZrO3RTrhpXz6h019JxOmjapNLT0tN7CwC7AEh2dFRSrvpyiJRVTautje9UDcnQlg_-QrBdl4R4TmsYZ3M8yxTjEdAbmFca8CT1zaSoyYQaEdWOtbct3jmU3fup63aMS3ehHg350rR8dDcjW6pmThu3jUumPqMKVJDJ11zfK-VS3jq9zb2HJyS2EsU6AQxh4uSiyWSJNJkIhBuQVGoBGLo4CD_tMzbKq9Oj7N70jU2SvgyB9QN62Qr6Eb7CmzZ2AkUD6rp7kZk8SVGT7zZ2d6XayqvS5aw3Iy1UzPokH8ApXLlFGcOxDgsyjxixX381VwqXk0KJ6BtsbmH5LMTuuqcwh-IyQj_fJ5e_1gtwaHo739f7oYO8puR3VLiUCpjbJ-mK-dM8gMFxkz2tvpOTHVbv_PzakdRY
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Helminth-derived+proteins+as+immune+system+regulators%3A+a+systematic+review+of+their+promise+in+alleviating+colitis&rft.jtitle=BMC+immunology&rft.au=Maimonah+Alghanmi&rft.au=Faisal+Minshawi&rft.au=Tarfa+A.+Altorki&rft.au=Ayat+Zawawi&rft.date=2024-04-18&rft.pub=BMC&rft.eissn=1471-2172&rft.volume=25&rft.issue=1&rft.spage=1&rft.epage=10&rft_id=info:doi/10.1186%2Fs12865-024-00614-2&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_dfc1143c059e4f4aa94b22cb67ab4044
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-2172&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-2172&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-2172&client=summon