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Molecular profiling of rheumatoid arthritis patients reveals an association between innate and adaptive cell populations and response to anti-tumor necrosis factor.
Farutin, Victor; Prod'homme, Thomas; McConnell, Kevin; Washburn, Nathaniel; Halvey, Patrick; Etzel, Carol J; Guess, Jamey; Duffner, Jay; Getchell, Kristen; Meccariello, Robin; Gutierrez, Bryan; Honan, Christopher; Zhao, Ganlin; Cilfone, Nicholas A; Gunay, Nur Sibel; Hillson, Jan L; DeLuca, David S; Saunders, Katherine C; Pappas, Dimitrios A; Greenberg, Jeffrey D; Kremer, Joel M; Manning, Anthony M; Ling, Leona E; Capila, Ishan.
Afiliación
  • Farutin V; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Prod'homme T; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • McConnell K; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Washburn N; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Halvey P; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Etzel CJ; Corrona LLC, Waltham, MA, USA.
  • Guess J; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Duffner J; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Getchell K; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Meccariello R; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Gutierrez B; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Honan C; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Zhao G; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Cilfone NA; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Gunay NS; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • Hillson JL; Momenta Pharmaceuticals Inc., 301 Binney Street, Cambridge, MA, 02142, USA.
  • DeLuca DS; DeLuca Data Science, Wietze, Germany.
  • Saunders KC; Corrona LLC, Waltham, MA, USA.
  • Pappas DA; Corrona LLC, Waltham, MA, USA.
  • Greenberg JD; Department of Medicine, Division of Rheumatology, Columbia University School of Medicine, New York, NY, USA.
  • Kremer JM; Corrona LLC, Waltham, MA, USA.
  • Manning AM; New York University School of Medicine, New York, NY, USA.
  • Ling LE; Corrona LLC, Waltham, MA, USA.
  • Capila I; Albany Medical College, Albany, NY, USA.
Arthritis Res Ther ; 21(1): 216, 2019 10 23.
Article en En | MEDLINE | ID: mdl-31647025
ABSTRACT

BACKGROUND:

The goal of this study is to use comprehensive molecular profiling to characterize clinical response to anti-TNF therapy in a real-world setting and identify reproducible markers differentiating good responders and non-responders in rheumatoid arthritis (RA).

METHODS:

Whole-blood mRNA, plasma proteins, and glycopeptides were measured in two cohorts of biologic-naïve RA patients (n = 40 and n = 36) from the Corrona CERTAIN (Comparative Effectiveness Registry to study Therapies for Arthritis and Inflammatory coNditions) registry at baseline and after 3 months of anti-TNF treatment. Response to treatment was categorized by EULAR criteria. A cell type-specific data analysis was conducted to evaluate the involvement of the most common immune cell sub-populations. Findings concordant between the two cohorts were further assessed for reproducibility using selected NCBI-GEO datasets and clinical laboratory measurements available in the CERTAIN database.

RESULTS:

A treatment-related signature suggesting a reduction in neutrophils, independent of the status of response, was indicated by a high level of correlation (ρ = 0.62; p < 0.01) between the two cohorts. A baseline, response signature of increased innate cell types in responders compared to increased adaptive cell types in non-responders was identified in both cohorts. This result was further assessed by applying the cell type-specific analysis to five other publicly available RA datasets. Evaluation of the neutrophil-to-lymphocyte ratio at baseline in the remaining patients (n = 1962) from the CERTAIN database confirmed the observation (odds ratio of good/moderate response = 1.20 [95% CI = 1.03-1.41, p = 0.02]).

CONCLUSION:

Differences in innate/adaptive immune cell type composition at baseline may be a major contributor to response to anti-TNF treatment within the first 3 months of therapy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / Factor de Necrosis Tumoral alfa / Perfilación de la Expresión Génica / Inmunidad Adaptativa / Inmunidad Innata Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Arthritis Res Ther Asunto de la revista: REUMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / Factor de Necrosis Tumoral alfa / Perfilación de la Expresión Génica / Inmunidad Adaptativa / Inmunidad Innata Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Arthritis Res Ther Asunto de la revista: REUMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos