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Banff Human Organ Transplant Transcripts Correlate with Renal Allograft Pathology and Outcome: Importance of Capillaritis and Subpathologic Rejection.
Rosales, Ivy A; Mahowald, Grace K; Tomaszewski, Kristen; Hotta, Kiyohiko; Iwahara, Naoya; Otsuka, Takuya; Tsuji, Takahiro; Takada, Yusuke; Acheampong, Ellen; Araujo-Medina, Milagros; Bruce, Amy; Rios, Andrea; Cosimi, Anthony Benedict; Elias, Nahel; Kawai, Tatsuo; Gilligan, Hannah; Safa, Kassem; Riella, Leonardo V; Tolkoff-Rubin, Nina E; Williams, Winfred W; Smith, Rex Neal; Colvin, Robert B.
Afiliación
  • Rosales IA; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Mahowald GK; Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Tomaszewski K; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Hotta K; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Iwahara N; Department of Urology, Hokkaido University Hospital, Hokkaido, Japan.
  • Otsuka T; Department of Urology, Hokkaido University Hospital, Hokkaido, Japan.
  • Tsuji T; Department of Surgical Pathology, Hokkaido University Hospital, Hokkaido, Japan.
  • Takada Y; Department of Pathology, Sapporo City General Hospital, Hokkaido, Japan.
  • Acheampong E; Department of Kidney Transplant Surgery, Sapporo City General Hospital, Hokkaido, Japan.
  • Araujo-Medina M; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Bruce A; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Rios A; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Cosimi AB; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Elias N; Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Kawai T; Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Gilligan H; Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Safa K; Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Riella LV; Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Tolkoff-Rubin NE; Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Williams WW; Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Smith RN; Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Colvin RB; Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
J Am Soc Nephrol ; 33(12): 2306-2319, 2022 12.
Article en En | MEDLINE | ID: mdl-36450597
ABSTRACT

BACKGROUND:

To seek insights into the pathogenesis of chronic active antibody-mediated rejection (CAMR), we performed mRNA analysis and correlated transcripts with pathologic component scores and graft outcomes.

METHODS:

We utilized the NanoString nCounter platform and the Banff Human Organ Transplant gene panel to quantify transcripts on 326 archived renal allograft biopsy samples. This system allowed correlation of transcripts with Banff pathology scores from the same tissue block and correlation with long-term outcomes.

RESULTS:

The only pathology score that correlated with AMR pathways in CAMR was peritubular capillaritis (ptc). C4d, cg, g, v, i, t, or ci scores did not correlate. DSA-negative CAMR had lower AMR pathway scores than DSA-positive CAMR. Transcript analysis in non-CAMR biopsies yielded evidence of increased risk of later CAMR. Among 108 patients without histologic CAMR, 23 developed overt biopsy-documented CAMR within 5 years and as a group had higher AMR pathway scores (P=3.4 × 10-5). Random forest analysis correlated 3-year graft loss with elevated damage, innate immunity, and macrophage pathway scores in CAMR and TCMR. Graft failure in CAMR was associated with TCMR transcripts but not with AMR transcripts, and graft failure in TCMR was associated with AMR transcripts but not with TCMR transcripts.

CONCLUSIONS:

Peritubular capillary inflammation and DSA are the primary drivers of AMR transcript elevation. Transcripts revealed subpathological evidence of AMR, which often preceded histologic CAMR and subpathological evidence of TCMR that predicted graft loss in CAMR.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Vasculares / Trasplante de Órganos / Trasplante de Riñón Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Vasculares / Trasplante de Órganos / Trasplante de Riñón Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Am Soc Nephrol Asunto de la revista: NEFROLOGIA Año: 2022 Tipo del documento: Article