Limits...
Low numbers of blood and salivary natural killer cells are associated with a better response to belimumab in primary Sjögren's syndrome: results of the BELISS study.

Seror R, Nocturne G, Lazure T, Hendel-Chavez H, Desmoulins F, Belkhir R, Ravaud P, Benbijja M, Poirier-Colame V, Taoufik Y, Mariette X - Arthritis Res. Ther. (2015)

Bottom Line: The median percentage of BAFF-positive cells in foci significantly decreased from 27.5 % (10-40) to 5 % (0-20) (p=0.03).Serum BAFF levels did not influence response to treatment.Low blood and salivary NK cell numbers are associated with a better response to belimumab.

View Article: PubMed Central - PubMed

Affiliation: Université Paris-Sud, Center of Research on Immunology of Viral and Autoimmune diseases (IMVA), INSERM U1184, Le Kremlin Bicêtre, France. raphaele.se@gmail.com.

ABSTRACT

Introduction: In this study, we sought to address changes in blood lymphocyte subpopulations and labial salivary gland (LSG) inflammation after belimumab treatment in patients with primary Sjögren's syndrome (pSS) and to identify predictors of response to treatment.

Methods: Sequential blood lymphocyte subsets and LSG biopsies were analysed between week 0 (W0) and W28 in 15 patients with pSS treated with belimumab. Systemic response to treatment was defined as a decrease in the European League Against Rheumatism Sjögren's Syndrome Disease Activity Index score of ≥3 points at W28.

Results: After belimumab, we observed a decrease in blood B lymphocytes primarily involving CD27-negative/immunoglobulin D-positive naïve B cells (p=0.008). Lymphocytic sialadenitis (focus score >1) that was present in 12 patients (80.0 %) before belimumab treatment became negative in 5 of them after treatment (p=0.03). The median (interquartile range) LSG B-cell/T-cell ratio decreased from 0.58 (0.5-0.67) to 0.50 (0.5-0.5) (p=0.06). B-cell activating factor (BAFF) staining was detected in 11 (78.6 %) of 14 patients before belimumab treatment compared with 7 (50.0 %) of 14 after belimumab therapy (p=0.10). The median percentage of BAFF-positive cells in foci significantly decreased from 27.5 % (10-40) to 5 % (0-20) (p=0.03). A systemic response was achieved in six patients (40 %). The only predictor of response was the presence of a low number of natural killer (NK) cells, both in blood (8.5 % [7-10] vs 11 % [9-21]; p=0.04) and in LSG (20.6/mm(3) [20.0-21.4] vs 30.0/mm(3) [25.0-100.0], p=0.003). Serum BAFF levels did not influence response to treatment.

Conclusions: Low blood and salivary NK cell numbers are associated with a better response to belimumab. This suggests that two distinct subsets of pSS may exist: one with a predominant type I interferon (IFN)-BAFF-B-cell axis, representing good responders to belimumab; and one with a predominant type II IFN-NK cell axis, representing non-responders.

Trial registration: ClinicalTrials.gov identifier: NCT01160666 . Registered 9 July 2010.

No MeSH data available.


Related in: MedlinePlus

Changes in natural killer (NK) cell count and proportion in responders and non-responders. Number (upper plot) and percentage (lower plot) of NK cells in responders and non-responders are shown. *p<0.05
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

License 1 - License 2
getmorefigures.php?uid=PMC4559969&req=5

Fig2: Changes in natural killer (NK) cell count and proportion in responders and non-responders. Number (upper plot) and percentage (lower plot) of NK cells in responders and non-responders are shown. *p<0.05

Mentions: This decrease primarily involved CD27−IgD+ naïve B cells (151 [24–186] at W0 vs 10 [6–40] at W28, n=9; p=0.008). There was no significant change in the total number of CD27+ memory B cells (39.5 [10.1–53.2] at W0 vs 47.7 [19.1–64.9] at W28, n=9; p=0.074) or CD27+IgD+ unswitched memory B cells (8.8 [3.4–28.9] at W0 vs 15.7 [6.6–28.8] at W28, n=9; p=0.36), but there was a slight increase in the number of CD27+IgD− switched memory B cells at W28 (19.6 [6.7–30.3] at W0 vs 35.8 [12.5–38.2] at W28; p=0.019) (Fig. 2).Fig. 2


Low numbers of blood and salivary natural killer cells are associated with a better response to belimumab in primary Sjögren's syndrome: results of the BELISS study.

Seror R, Nocturne G, Lazure T, Hendel-Chavez H, Desmoulins F, Belkhir R, Ravaud P, Benbijja M, Poirier-Colame V, Taoufik Y, Mariette X - Arthritis Res. Ther. (2015)

Changes in natural killer (NK) cell count and proportion in responders and non-responders. Number (upper plot) and percentage (lower plot) of NK cells in responders and non-responders are shown. *p<0.05
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

License 1 - License 2
Show All Figures
getmorefigures.php?uid=PMC4559969&req=5

Fig2: Changes in natural killer (NK) cell count and proportion in responders and non-responders. Number (upper plot) and percentage (lower plot) of NK cells in responders and non-responders are shown. *p<0.05
Mentions: This decrease primarily involved CD27−IgD+ naïve B cells (151 [24–186] at W0 vs 10 [6–40] at W28, n=9; p=0.008). There was no significant change in the total number of CD27+ memory B cells (39.5 [10.1–53.2] at W0 vs 47.7 [19.1–64.9] at W28, n=9; p=0.074) or CD27+IgD+ unswitched memory B cells (8.8 [3.4–28.9] at W0 vs 15.7 [6.6–28.8] at W28, n=9; p=0.36), but there was a slight increase in the number of CD27+IgD− switched memory B cells at W28 (19.6 [6.7–30.3] at W0 vs 35.8 [12.5–38.2] at W28; p=0.019) (Fig. 2).Fig. 2

Bottom Line: The median percentage of BAFF-positive cells in foci significantly decreased from 27.5 % (10-40) to 5 % (0-20) (p=0.03).Serum BAFF levels did not influence response to treatment.Low blood and salivary NK cell numbers are associated with a better response to belimumab.

View Article: PubMed Central - PubMed

Affiliation: Université Paris-Sud, Center of Research on Immunology of Viral and Autoimmune diseases (IMVA), INSERM U1184, Le Kremlin Bicêtre, France. raphaele.se@gmail.com.

ABSTRACT

Introduction: In this study, we sought to address changes in blood lymphocyte subpopulations and labial salivary gland (LSG) inflammation after belimumab treatment in patients with primary Sjögren's syndrome (pSS) and to identify predictors of response to treatment.

Methods: Sequential blood lymphocyte subsets and LSG biopsies were analysed between week 0 (W0) and W28 in 15 patients with pSS treated with belimumab. Systemic response to treatment was defined as a decrease in the European League Against Rheumatism Sjögren's Syndrome Disease Activity Index score of ≥3 points at W28.

Results: After belimumab, we observed a decrease in blood B lymphocytes primarily involving CD27-negative/immunoglobulin D-positive naïve B cells (p=0.008). Lymphocytic sialadenitis (focus score >1) that was present in 12 patients (80.0 %) before belimumab treatment became negative in 5 of them after treatment (p=0.03). The median (interquartile range) LSG B-cell/T-cell ratio decreased from 0.58 (0.5-0.67) to 0.50 (0.5-0.5) (p=0.06). B-cell activating factor (BAFF) staining was detected in 11 (78.6 %) of 14 patients before belimumab treatment compared with 7 (50.0 %) of 14 after belimumab therapy (p=0.10). The median percentage of BAFF-positive cells in foci significantly decreased from 27.5 % (10-40) to 5 % (0-20) (p=0.03). A systemic response was achieved in six patients (40 %). The only predictor of response was the presence of a low number of natural killer (NK) cells, both in blood (8.5 % [7-10] vs 11 % [9-21]; p=0.04) and in LSG (20.6/mm(3) [20.0-21.4] vs 30.0/mm(3) [25.0-100.0], p=0.003). Serum BAFF levels did not influence response to treatment.

Conclusions: Low blood and salivary NK cell numbers are associated with a better response to belimumab. This suggests that two distinct subsets of pSS may exist: one with a predominant type I interferon (IFN)-BAFF-B-cell axis, representing good responders to belimumab; and one with a predominant type II IFN-NK cell axis, representing non-responders.

Trial registration: ClinicalTrials.gov identifier: NCT01160666 . Registered 9 July 2010.

No MeSH data available.


Related in: MedlinePlus