Analyze Diet
The Journal of general virology2007; 89(Pt 1); 138-147; doi: 10.1099/vir.0.83266-0

Immunotherapy of equine sarcoid: dose-escalation trial for the use of chimeric papillomavirus-like particles.

Abstract: Equine sarcoids are fibrosarcoma-like skin tumours with a prevalence of approximately 1-2 %. Strong evidence exists for a causative role of bovine papillomavirus (BPV) type 1 or type 2 in the development of sarcoids. No effective treatment of equine sarcoid is available and after surgical excision relapse of the tumours is very frequent. We developed chimeric virus-like particles (CVLPs) of BPV 1 L1-E7 for the immunotherapy of equine sarcoid. In a phase I clinical trial 12 horses suffering from equine sarcoid with an average number of more than 22 tumours per animal were vaccinated in a dose-escalation setting. The animals were followed-up for 63 days, eight of the twelve horses were followed-up for more than a year and side-effects, humoral immune responses and tumour appearance were recorded. BPV DNA was detected in tumours of 11 cases. CVLPs were well tolerated in all dose groups, a robust anti-L1 antibody response was induced in all but one of the horses. Anti-E7 antibodies were detected in five of the 12 animals at low titres. Two animals showed a clear improvement of the clinical status after treatment, i.e. the number of the tumours per horse was reduced. In another horse regression of five sarcoids was observed; three of them relapsed during the study. Two animals showed tumour regression as well as growth of new sarcoids. In two horses the clinical status remained unchanged, in another two horses growth of existing tumours or growth of additional tumours was observed. The remaining three animals showed simultaneously regression and growth of existing tumours. Neither the humoral immune responses nor the observed effects on the tumours was correlated with the dose group.
Publication Date: 2007-12-20 PubMed ID: 18089737DOI: 10.1099/vir.0.83266-0Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research study investigates the possibility of using immunotherapy to treat equine sarcoids, a common type of skin tumor in horses, with virus-like particles that are genetically engineered versions of bovine papillomavirus. The results from a trial involving twelve horses showed a reduction in tumor numbers in some cases, but it was unclear whether there was a correlation between dosages used and responses observed.

Objective and Background of the Research

  • The research primarily aims at evaluating the efficacy of using chimeric virus-like particles (CVLPs) from bovine papillomavirus (BPV) type 1 L1-E7 for the immunotherapy of equine sarcoid.
  • Equine sarcoids are a type of common skin tumor found in horses that often relapse after surgical removal. These tumors are linked to infection by bovine papillomavirus (BPV) type 1 or type 2.
  • To date, no effective treatment method has been established for these tumors. Therefore, this research may pave the way for a novel approach to treating these tumors using immunotherapy.

Design and Methodology

  • The research was performed as a small-scale clinical trial, or phase I, on a group of twelve horses suffering from equine sarcoids. These horses had an average of over 22 tumors each.
  • The trial followed a dose-escalation design, meaning the dosage of the CVLPs was gradually increased during the trial.

Results and Findings

  • The CVLPs were well tolerated in all dose groups, and a strong anti-L1 antibody response was seen except for in one horse.
  • Out of the 12 horses, Anti-E7 antibodies were detected in five, featuring low titres. However, it was unclear whether the presence of these antibodies correlated with any clinical improvement.
  • Two horses showed a significant reduction in tumor numbers, whereas five tumors regressed in a single horse; three of these five later relapsed.
  • In two horses the condition remained unchanged, while in another two horses there was growth of existing tumors or growth of new tumors. Meanwhile, the remaining three horses demonstrated both regression and growth of existing tumors simultaneously.

Interpretation and Conclusion

  • The main conclusion from the trial is that immunotherapy using CVLPs shows potential as a treatment for equine sarcoids.
  • The research did not establish a clear correlation between the dose group and the observed effects on the tumors or the humoral immune responses.
  • While certain promising findings are presented, the diverse responses and the relapse in some horses point towards a need for further research. The study’s findings indicate that the treatment process could be more complex than anticipated and might require a tailored approach for each individual case.

Cite This Article

APA
Mattil-Fritz S, Scharner D, Piuko K, Thönes N, Gissmann L, Müller H, Müller M. (2007). Immunotherapy of equine sarcoid: dose-escalation trial for the use of chimeric papillomavirus-like particles. J Gen Virol, 89(Pt 1), 138-147. https://doi.org/10.1099/vir.0.83266-0

Publication

ISSN: 0022-1317
NlmUniqueID: 0077340
Country: England
Language: English
Volume: 89
Issue: Pt 1
Pages: 138-147

Researcher Affiliations

Mattil-Fritz, Stephanie
  • Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.
Scharner, Doreen
  • Universität Leipzig, Veterinärmedizinische Fakultät, Chirurgische Tierklinik, Leipzig, Germany.
Piuko, Konrad
  • Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.
Thönes, Nadja
  • Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.
Gissmann, Lutz
  • Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.
Müller, Hermann
  • Universität Leipzig, Veterinärmedizinische Fakultät, Institut für Virologie Leipzig, Germany.
Müller, Martin
  • Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.

MeSH Terms

  • Animals
  • Antibodies, Viral / analysis
  • Antibody Formation
  • Biopsy
  • Bovine papillomavirus 1 / genetics
  • Bovine papillomavirus 1 / isolation & purification
  • Chimera
  • DNA, Viral / genetics
  • DNA, Viral / isolation & purification
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Fibrosarcoma / immunology
  • Fibrosarcoma / surgery
  • Fibrosarcoma / veterinary
  • Fibrosarcoma / virology
  • Horse Diseases / immunology
  • Horse Diseases / surgery
  • Horse Diseases / virology
  • Horses
  • Immunotherapy
  • Male
  • Papillomavirus Infections / immunology
  • Papillomavirus Infections / surgery
  • Papillomavirus Infections / veterinary
  • Recurrence
  • Sarcoidosis / immunology
  • Sarcoidosis / surgery
  • Sarcoidosis / veterinary
  • Sarcoidosis / virology

Citations

This article has been cited 6 times.
  1. Jindra C, Hainisch EK, Brandt S. Immunotherapy of Equine Sarcoids-From Early Approaches to Innovative Vaccines. Vaccines (Basel) 2023 Mar 30;11(4).
    doi: 10.3390/vaccines11040769pubmed: 37112681google scholar: lookup
  2. Hainisch EK, Jindra C, Kirnbauer R, Brandt S. Papillomavirus-like Particles in Equine Medicine. Viruses 2023 Jan 25;15(2).
    doi: 10.3390/v15020345pubmed: 36851559google scholar: lookup
  3. Wilson AD, Hicks C. Both tumour cells and infiltrating T-cells in equine sarcoids express FOXP3 associated with an immune-supressed cytokine microenvironment. Vet Res 2016 May 9;47(1):55.
    doi: 10.1186/s13567-016-0339-8pubmed: 27160146google scholar: lookup
  4. Hainisch EK, Brandt S, Shafti-Keramat S, Van den Hoven R, Kirnbauer R. Safety and immunogenicity of BPV-1 L1 virus-like particles in a dose-escalation vaccination trial in horses. Equine Vet J 2012 Jan;44(1):107-11.
  5. Jia R, Cheng A, Wang M, Qi X, Zhu D, Ge H, Luo Q, Liu F, Guo Y, Chen X. Development and evaluation of an antigen-capture ELISA for detection of the UL24 antigen of the duck enteritis virus, based on a polyclonal antibody against the UL24 expression protein. J Virol Methods 2009 Oct;161(1):38-43.
  6. Smith CH, Stewart HL, Stefanovski D, Levine DG. Outcomes following autologous tumor tissue implantation with or without concurrent antineoplastic therapies in the treatment of sarcoids in 50 equids. Front Vet Sci 2025;12:1559519.
    doi: 10.3389/fvets.2025.1559519pubmed: 40417356google scholar: lookup