Immune response by host after allogeneic chondrocyte transplant to the cartilage
- PMID: 12112416
- DOI: 10.1002/jemt.10110
Immune response by host after allogeneic chondrocyte transplant to the cartilage
Abstract
Chondrocytes constitutively express class I and, in some species, class II major histocompatibility complex (MHC). It is also possible that they possess specific differentiation antigen(s). Furthermore, lymphocytic cells, corresponding to NK cells, display spontaneous cytotoxic activity against chondrocytes. Studies on articular cartilage repair by transplants of allogeneic chondrocytes were mainly done on non-inbred animals, such as rabbits and hens. Surprisingly, only in single instances these transplants were rejected. In inbred rats, allogeneic chondrocytes transplanted into full-thickness defects in articular cartilage immediately after isolation evoked systemic immunological reaction and produced cartilage was rejected. Combined immunosuppression with cyclosporin A and cladribine did not prevent rejection of such transplants. Mechanical separation of transplants from bone marrow prevented sensitization of recipients and rejection of the produced cartilage. Successful allogeneic chondrocyte transplants in rabbits and hens could be tentatively explained by a certain degree of inbreeding among experimental animals, by the use of chondrocytes cultivated before grafting in artificial scaffolds and thus protected by matrix produced in vitro, and also by creation of a temporary mechanical barrier between transplant and bone marrow by tissues damaged during preparation of the defect.
Copyright 2002 Wiley-Liss, Inc.
Similar articles
-
Cartilage formed by syngeneic rat chondrocytes in joint surface defects is rejected in animals sensitized with allogeneic chondrocytes: involvement of the synovial lining.Arch Immunol Ther Exp (Warsz). 2005 Mar-Apr;53(2):159-68. Arch Immunol Ther Exp (Warsz). 2005. PMID: 15928585
-
Immunosuppression and rejection of cartilage formed by allogeneic chondrocytes in rats.Cell Transplant. 1999 Nov-Dec;8(6):627-36. doi: 10.1177/096368979900800609. Cell Transplant. 1999. PMID: 10701492
-
Cartilage produced after transplantation of syngeneic chondrocytes is rejected in rats presensitized with allogeneic chondrocytes.Cell Transplant. 2001;10(7):625-32. Cell Transplant. 2001. PMID: 11714197
-
Antigenic and immunogenic properties of chondrocytes. Implications for chondrocyte therapeutic transplantation and pathogenesis of inflammatory and degenerative joint diseases.Cent Eur J Immunol. 2018;43(2):209-219. doi: 10.5114/ceji.2018.77392. Epub 2018 Jun 30. Cent Eur J Immunol. 2018. PMID: 30135635 Free PMC article. Review.
-
Cartilage repair: generations of autologous chondrocyte transplantation.Eur J Radiol. 2006 Jan;57(1):24-31. doi: 10.1016/j.ejrad.2005.08.009. Epub 2005 Sep 26. Eur J Radiol. 2006. PMID: 16188417 Review.
Cited by
-
miR-103a-3p and miR-22-5p Are Reliable Reference Genes in Extracellular Vesicles From Cartilage, Adipose Tissue, and Bone Marrow Cells.Front Bioeng Biotechnol. 2021 Feb 15;9:632440. doi: 10.3389/fbioe.2021.632440. eCollection 2021. Front Bioeng Biotechnol. 2021. PMID: 33659243 Free PMC article.
-
Bioengineered chondrocyte-products from human induced pluripotent stem cells are useful for repairing articular cartilage injury in minipig model.NPJ Regen Med. 2025 Jul 1;10(1):31. doi: 10.1038/s41536-025-00420-3. NPJ Regen Med. 2025. PMID: 40593743 Free PMC article.
-
Long-Term Results of Cartilage Repair after Allogeneic Transplantation of Cartilaginous Aggregates Formed from Bone Marrow-Derived Cells for Large Osteochondral Defects in Rabbit Knees.Cartilage. 2013 Oct;4(4):339-44. doi: 10.1177/1947603513494003. Cartilage. 2013. PMID: 26069678 Free PMC article.
-
Success rates and immunologic responses of autogenic, allogenic, and xenogenic treatments to repair articular cartilage defects.Tissue Eng Part B Rev. 2009 Mar;15(1):1-15. doi: 10.1089/ten.teb.2008.0189. Tissue Eng Part B Rev. 2009. PMID: 19063664 Free PMC article. Review.
-
Genetic engineering of juvenile human chondrocytes improves scaffold-free mosaic neocartilage grafts.Clin Orthop Relat Res. 2013 Jan;471(1):26-38. doi: 10.1007/s11999-012-2615-x. Epub 2012 Sep 25. Clin Orthop Relat Res. 2013. PMID: 23008026 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials