Increased B Cell and Cytotoxic NK Cell Proportions and Increased T Cell Responsiveness in Blood of Natalizumab-Treated Multiple Sclerosis PatientsShow others and affiliations
2013 (English)In: PLOS ONE, E-ISSN 1932-6203, Vol. 8, no 12, article id e81685
Article in journal (Refereed) Published
Abstract [en]
Background: Changes in the blood lymphocyte composition probably both mediate and reflect the effects of natalizumab treatment in multiple sclerosis, with implications for treatment benefits and risks.
Methods: A broad panel of markers for lymphocyte populations, including states of activation and co-stimulation, as well as functional T cell responses to recall antigens and mitogens, were assessed by flow cytometry in 40 patients with relapsing multiple sclerosis before and after one-year natalizumab treatment.
Results: Absolute numbers of all major lymphocyte populations increased after treatment, most markedly for NK and B cells. The fraction of both memory and presumed regulatory B cell subsets increased, as did CD3(-)CD56(dim) cytotoxic NK cells, whereas CD3(-)CD56(bright) regulatory NK cells decreased. The increase in cell numbers was further associated with a restored T cell responsiveness to recall antigens and mitogens in functional assays.
Conclusions: Our data confirms that natalizumab treatment increases the number of lymphocytes in blood, likely mirroring the expression of VLA-4 being highest on NK and B cells. This finding supports reduction of lymphocyte extravasation as a main mode of action, although the differential effects on subpopulation composition suggests that cell-signalling may also be affected. The systemic increase in T cell responsiveness reflects the increase in numbers, and while augmenting anti-infectious responses systemically, localized responses may become correspondingly decreased.
Place, publisher, year, edition, pages
PLOS , 2013. Vol. 8, no 12, article id e81685
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:oru:diva-97551DOI: 10.1371/journal.pone.0081685ISI: 000327944500088PubMedID: 24312575Scopus ID: 2-s2.0-8489142012OAI: oai:DiVA.org:oru-97551DiVA, id: diva2:1638199
Funder
Swedish Association of Persons with Neurological DisabilitiesLinköpings universitet
Note
Funding agencies:
University Hospital of Linköping
County Council of östergätland
Biogen Idec Sweden
2022-02-162022-02-162025-02-18Bibliographically approved