-
Je něco špatně v tomto záznamu ?
A 2-fold Approach to Polyoma Virus (BK) Nephropathy in Kidney Transplants: Distinguishing Direct Virus Effects From Cognate T Cell-mediated Inflammation
PF. Halloran, KS. Madill-Thomsen, GA. Böhmig, M. Myslak, G. Gupta, D. Kumar, O. Viklicky, A. Perkowska-Ptasinska, KS. Famulski, INTERCOMEX Investigators
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- biopsie MeSH
- lidé MeSH
- Polyomavirus * MeSH
- rejekce štěpu MeSH
- T-lymfocyty MeSH
- transplantace ledvin * škodlivé účinky MeSH
- zánět diagnóza MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
BACKGROUND: BK nephropathy (BKN) in kidney transplants diagnosed by histology is challenging because it involves damage from both virus activity and cognate T cell-mediated inflammation, directed against alloantigens (rejection) or viral antigens. The present study of indication biopsies from the Integrated Diagnostic System in the International Collaborative Microarray Study Extension study measured major capsid viral protein 2 (VP2) mRNA to assess virus activity and a T cell-mediated rejection (TCMR) classifier to assess cognate T cell-mediated inflammation. METHODS: Biopsies were assessed by local standard-of-care histology and by genome-wide microarrays and Molecular Microscope Diagnostic System (MMDx) algorithms to detect rejection and injury. In a subset of 102 biopsies (50 BKN and 52 BKN-negative biopsies with various abnormalities), we measured VP2 transcripts by real-time polymerase chain reaction. RESULTS: BKN was diagnosed in 55 of 1679 biopsies; 30 had cognate T cell-mediated activity assessed by by MMDx and TCMR lesions, but only 3 of 30 were histologically diagnosed as TCMR. We developed a BKN probability classifier that predicted histologic BKN (area under the curve = 0.82). Virus activity (VP2 expression) was highly selective for BKN (area under the curve = 0.94) and correlated with acute injury, atrophy-fibrosis, macrophage activation, and the BKN classifier, but not with the TCMR classifier. BKN with molecular TCMR had more tubulitis and inflammation than BKN without molecular TCMR. In 5 BKN cases with second biopsies, VP2 mRNA decreased in second biopsies, whereas in 4 of 5 TCMR classifiers, scores increased. Genes and pathways associated with BKN and VP2 mRNA were similar, reflecting injury, inflammation, and macrophage activation but none was selective for BKN. CONCLUSIONS: Risk-benefit decisions in BKN may be assisted by quantitative assessment of the 2 major pathologic processes, virus activity and cognate T cell-mediated inflammation.
Alberta Transplant Applied Genomics Centre Edmonton AB Canada
Department of Pathology Medical University of Warsaw Warsaw Poland
Division of Nephrology Virginia Commonwealth University Richmond VA
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22019652
- 003
- CZ-PrNML
- 005
- 20220804135850.0
- 007
- ta
- 008
- 220720s2021 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1097/TP.0000000000003884 $2 doi
- 035 __
- $a (PubMed)34310102
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Halloran, Philip F $u Alberta Transplant Applied Genomics Centre, Edmonton, AB, Canada $u Department of Medicine, Division of Nephrology and Transplant Immunology, University of Alberta, Edmonton, AB, Canada
- 245 12
- $a A 2-fold Approach to Polyoma Virus (BK) Nephropathy in Kidney Transplants: Distinguishing Direct Virus Effects From Cognate T Cell-mediated Inflammation / $c PF. Halloran, KS. Madill-Thomsen, GA. Böhmig, M. Myslak, G. Gupta, D. Kumar, O. Viklicky, A. Perkowska-Ptasinska, KS. Famulski, INTERCOMEX Investigators
- 520 9_
- $a BACKGROUND: BK nephropathy (BKN) in kidney transplants diagnosed by histology is challenging because it involves damage from both virus activity and cognate T cell-mediated inflammation, directed against alloantigens (rejection) or viral antigens. The present study of indication biopsies from the Integrated Diagnostic System in the International Collaborative Microarray Study Extension study measured major capsid viral protein 2 (VP2) mRNA to assess virus activity and a T cell-mediated rejection (TCMR) classifier to assess cognate T cell-mediated inflammation. METHODS: Biopsies were assessed by local standard-of-care histology and by genome-wide microarrays and Molecular Microscope Diagnostic System (MMDx) algorithms to detect rejection and injury. In a subset of 102 biopsies (50 BKN and 52 BKN-negative biopsies with various abnormalities), we measured VP2 transcripts by real-time polymerase chain reaction. RESULTS: BKN was diagnosed in 55 of 1679 biopsies; 30 had cognate T cell-mediated activity assessed by by MMDx and TCMR lesions, but only 3 of 30 were histologically diagnosed as TCMR. We developed a BKN probability classifier that predicted histologic BKN (area under the curve = 0.82). Virus activity (VP2 expression) was highly selective for BKN (area under the curve = 0.94) and correlated with acute injury, atrophy-fibrosis, macrophage activation, and the BKN classifier, but not with the TCMR classifier. BKN with molecular TCMR had more tubulitis and inflammation than BKN without molecular TCMR. In 5 BKN cases with second biopsies, VP2 mRNA decreased in second biopsies, whereas in 4 of 5 TCMR classifiers, scores increased. Genes and pathways associated with BKN and VP2 mRNA were similar, reflecting injury, inflammation, and macrophage activation but none was selective for BKN. CONCLUSIONS: Risk-benefit decisions in BKN may be assisted by quantitative assessment of the 2 major pathologic processes, virus activity and cognate T cell-mediated inflammation.
- 650 _2
- $a biopsie $7 D001706
- 650 _2
- $a rejekce štěpu $7 D006084
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a zánět $x diagnóza $7 D007249
- 650 12
- $a transplantace ledvin $x škodlivé účinky $7 D016030
- 650 12
- $a Polyomavirus $7 D011120
- 650 _2
- $a T-lymfocyty $7 D013601
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Madill-Thomsen, Katelynn S $u Alberta Transplant Applied Genomics Centre, Edmonton, AB, Canada
- 700 1_
- $a Böhmig, Georg A $u Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria
- 700 1_
- $a Myslak, Marek $u Department of Nephrology and Kidney Transplantation, SPWSZ Hospital in Szczecin, Pomeranian Medical University, Szczecin, Poland
- 700 1_
- $a Gupta, Gaurav $u Division of Nephrology, Virginia Commonwealth University, Richmond, VA
- 700 1_
- $a Kumar, Dhiren $u Division of Nephrology, Virginia Commonwealth University, Richmond, VA
- 700 1_
- $a Viklicky, Ondrej $u Department of Nephrology and Transplant Center, Institute for Clinical and Experimental Medicine, Prague, Czech Republic
- 700 1_
- $a Perkowska-Ptasinska, Agnieszka $u Department of Pathology, Medical University of Warsaw, Warsaw, Poland
- 700 1_
- $a Famulski, Konrad S $u Alberta Transplant Applied Genomics Centre, Edmonton, AB, Canada
- 710 2_
- $a INTERCOMEX Investigators
- 773 0_
- $w MED00010695 $t Transplantation $x 1534-6080 $g Roč. 105, č. 11 (2021), s. 2374-2384
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34310102 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220720 $b ABA008
- 991 __
- $a 20220804135844 $b ABA008
- 999 __
- $a ok $b bmc $g 1823027 $s 1170895
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 105 $c 11 $d 2374-2384 $e 20211101 $i 1534-6080 $m Transplantation $n Transplantation $x MED00010695
- LZP __
- $a Pubmed-20220720