4.7 Article

RNA-based immunoglobulin repertoire sequencing is a new tool for the management of monoclonal gammopathy of renal (kidney) significance

Journal

KIDNEY INTERNATIONAL
Volume 101, Issue 2, Pages 331-337

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2021.10.017

Keywords

AL-amyloidosis; Ig; monoclonal gammopathy of renal signifi-cance; next-generation sequencing

Funding

  1. Comite d'Orientation de la Recherche en Cancerologie (CORC)
  2. Limousin Committees of Ligue Nationale Contre le Cancer
  3. Agence Regionale de la Sante
  4. Institut Universitaire de France
  5. Association Francaise Contre l'Amylose
  6. Fondation Francaise pour la Recherche Contre le Myelome et les Gammapathies
  7. AREN Poitou-Charentes

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The study developed a high throughput sequencing assay to detect subtle clonal disorders in monoclonal gammopathy of renal significance, which could potentially improve the management of this kidney disease.
The diagnostic approach of monoclonal gammopathy of renal significance is based on the detection of a monoclonal immunoglobulin in the blood and urine, and the identification of the underlying clone through bone marrow and/or peripheral blood cytologic and flow cytometry analysis. However, the monoclonal component and its corresponding clone may be undetectable using these routine techniques. Since clone identification is the cornerstone for guiding therapy and assessing disease response, more sensitive methods are required. We recently developed a high throughput sequencing assay from bone marrow mRNA encoding immunoglobulins (RACE-RepSeq). This technique provides both full-length V(D)J region (variable, diversity and joining genes that generate unique receptors as antigen receptors) of the monoclonal immunoglobulin and the dominant immunoglobulin repertoire. This allows analysis of mutational patterns, immunoglobulin variable gene frequencies and diversity due to somatic hypermutation. Here, we evaluated the diagnostic performance of RACE-RepSeq in 16 patients with monoclonal-associated kidney lesions, and low serum monoclonal immunoglobulin and free light chain levels at diagnosis. Bone marrow immunohistochemical analysis was negative in all 11 patients so tested and 7 of 12 patients had no detectable clone matching the kidney deposits using flow cytometry analysis. By contrast, RACE-RepSeq detected a dominant clonal light chain sequence of matched isotype with respect to kidney deposits in all patients. Thus, high throughput mRNA sequencing appears highly sensitive to detect subtle clonal disorders in monoclonal gammopathy of renal significance and suggest this novel approach could help improve the management of this kidney disease.

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