Cited by 114Cytokine Signaling Pathways and InteractionsImmune Response and InflammationRheumatoid Arthritis Research and Therapies

Interleukin-10 potential benefits and possible risks in clinical infectious diseases

Opal, Steven M., Wherry, Janice C., Grint, Paul·1998·Clinical Infectious Diseases

Abstract

Human interleukin-10 (IL-10) is a potent anti-inflammatory cytokine that inhibits the synthesis of the major proinflammatory cytokines and chemokines. IL-10 is the principal TH2-type cytokine that upregulates humoral immune responses and attenuates cell-mediated immune reactions. This cytokine has a number of immunomodulatory properties that might be clinically useful in a variety of inflammatory and infectious disease states. Clinical trials with human recombinant IL-10 are already in progress. Carefully selected patients with inflammatory conditions may benefit from IL- 10 therapy if concomitant infectious diseases are recognized and treated appropriately.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1086/515032

Cites

92 of 92 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

2 of the 94 references couldn’t be matched to a known paper.

Research works printed but not linked: 15

  1. Corrall LG, Muller GW, Moreira AL, et al. Selection of novel analogues Exogenous IL-10 downregulates TNF, IL-1b, and IL-6 in pe- of thalidomide with enhanced tumor necrosis factor-a inhibitory activ- ripheral blood mononuclear cells in patients with ity. Mol Med 1996; 2:506 -15.
  2. Kim JM, Brannan CI, Copeland NG, Jenkins MA, Khan TA, Moore KW. [137]. It will be imperative to define and treat against clinically Structure of the mouse IL-10 gene and chromosomal location of the relevant microbial pathogens prior to use of this potent anti- mouse and human genes. J Immunol 1992; 148:3618 -23. inflammatory cytokine.
  3. Zdanov A, Schalk-Hihi C, Wlodawer A. Crystal structure of human 5. Davey RT Jr, Chaitt DG, Piscitelli SC, et al. Subcutaneous administration interleukin-10 at 1.6A and a model of a complex with its soluble of interleukin-2 in human immunodeficiency virus type I -infected persons. J Infect Dis 1997; 175:781 -9. receptor. Protein Sci 1996; 5:1955 -62. / 9c5c$$de27 11-13-98 16:39:06 cida UC: CID
  4. Klava A, Windsor AC, Farmery SM, et al. Interleukin-10: a role in the 48. Westendorp RGJ, Langermans JAM, Huizinga TWJ, et al. Genetic influ- development of post-operative immunosuppression. Arch Surg 1997; ence on cytokine production in fatal meningococcal disease. Lancet 1997; 349:170 -3. 132:425 -9. / 9c5c$$de27 11-13-98 16:39:06 cida UC: CID
  5. Fluckiger AC, Durand I, Banchereau J. Interleukin-10 induces apoptotic delaying mRNA degradation. J Exp Med 1994; 179:1695 -9.
  6. Opal SM. Lessons learned in recent clinical trials for sepsis. J Endotoxin Res 1995; 2:221 -6. 157:3672 -80.
  7. Taga K, Tosato G. IL-10 inhibits human T cell proliferation and IL-2 synthesis. J Immunol 1992; 148:1143 -8. 96:2339 -47.
  8. van der Poll T, Marchant A, Buurman W, et al. Endogenous interleukin- 74. Williams NG, Paradis H, Agarwal S, Charest DL, Pelech SL, Roberts TM. Raf-1 and p21 v-ras cooperate in the activation of mitogen-activated 10 protects mice from death during septic peritonitis. J Immunol 1995; 155:5397 -401. protein kinase. Proc Natl Acad Sci USA 1993; 90:5772 -6.
  9. Cusumano V, Genovese F, Mancuso G, Carbone M, Fera MT, Teti G. Biol Chem 1995; 270:9558 -63.
  10. Willems F, Marchant A, Delville JP, et al. Interleukin-10 inhibits B7 and intracellular adhesion molecule-1 expression on human monocytes. its cytokine responses in endotoxemia. Gene Ther 1997;4:140-9.
  11. Terminelli C, Denhardt G, Narula S, Thorbecke GJ. Administration of interleukin-10 at the time of priming protects Corynebacterium par- tion of a cerebrospinal fluid inhibitor of macrophage listericidal func- tion as interleukin-10. J Exp Med 1993; 178:1255 -61.
  12. Cavaillon J-M. Reduced cytokine production by circulating leukocytes 103. Yang X, HayGlass KT, Brunham RC. Genetically determined differences in IL-10 and IFN-gamma responses correlate with clearance of Chla- from patients with sepsis [abstract no S-13]. In: Program and abstracts of the 37th Interscience Conference on Antimicrobial Agents and Che- mydia trachomatis mouse peritonitis infection. J Immunol 1996; 156: 4338 -44.
  13. Greenberger MJ, Strieter RM, Kunkel SL, Danforth JM, Goodman RE, Standiford TJ. Neutralization of IL-10 increases survival in the murine Natl Acad Sci USA 1992; 85:1890 -8.
  14. Bellon JM, Manzano L, Bernardos L, et al. Cytokine levels after open and laproscopic cholecystectomy. Eur Surg Res 1997; 29:27 -34. 1998;178:520-5. 137. van de Poll T, Marchant A, van Deventer SJH. The role of interleukin- 123.
  15. Sherry RM, Cue JI, Goddard JK, Parramore JB, DiPiro JT. Interleukin- 10 is associated with the development of sepsis in trauma. J Trauma 10 in the pathogenesis of bacterial infection. Clin Microbiol Infect 1997; 3:605 -7. 1996; 40:616 -7.

Cited by

Sorted by citations

Authors
Opal, S. M., Wherry, J. C., & Grint, P.
Affiliations
  • Brown University (US)
  • Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
Corresponding author
Opal, Steven M.
Venue
Clinical Infectious Diseases
Published
1998-12-01
Volume
27
Issue
6
Pages
1497-1507
ISSN
  • 1058-4838 (ISSN-L)
  • 1537-6591
OpenAlex
W1985344660
Cited by
114
References
94
Citations by year
2025: 2 · 2023: 2 · 2021: 2 · 2020: 2 · 2019: 4 · 2018: 1 · 2017: 5 · 2016: 2 · 2015: 6 · 2014: 3 · 2013: 3 · 2012: 3
FWCI
0.77
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Infectious Diseases (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
  • Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
Keywords
IL-10, anti-inflammatory cytokines, immunomodulation, inflammatory cytokines, Th2 cytokines, humoral immune response, cell-mediated immunity, inflammatory diseases, infectious diseases, clinical trials
MeSH terms
Adjuvants, Immunologic, Animals, Anti-Inflammatory Agents, Non-Steroidal, Communicable Diseases, Humans, Interleukin-10, Receptors, Interleukin, Endotoxemia, Mice, Receptors, Interleukin-10

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