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Characterization of CD8 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis showing cell percentage of (a, g) CD8 + , (b, h) CD154 + , (c, i) <t>CD69</t> + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + in peripheral blood mononuclear cells (PBMCs) of (a-f) IFN- and (g-l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.
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Characterization of CD8 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis showing cell percentage of (a, g) CD8 + , (b, h) CD154 + , (c, i) <t>CD69</t> + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + in peripheral blood mononuclear cells (PBMCs) of (a-f) IFN- and (g-l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.
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Characterization of CD8 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis showing cell percentage of (a, g) CD8 + , (b, h) CD154 + , (c, i) <t>CD69</t> + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + in peripheral blood mononuclear cells (PBMCs) of (a-f) IFN- and (g-l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.
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Characterization of CD8 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis showing cell percentage of (a, g) CD8 + , (b, h) CD154 + , (c, i) CD69 + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + in peripheral blood mononuclear cells (PBMCs) of (a-f) IFN- and (g-l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.

Journal: Frontiers in Immunology

Article Title: Multiple sclerosis patients under treatment with interferon β1-a or ocrelizumab exhibit different T and B cell responses to SARS-CoV-2 vaccine

doi: 10.3389/fimmu.2026.1773417

Figure Lengend Snippet: Characterization of CD8 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis showing cell percentage of (a, g) CD8 + , (b, h) CD154 + , (c, i) CD69 + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + in peripheral blood mononuclear cells (PBMCs) of (a-f) IFN- and (g-l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.

Article Snippet: After the stimulation, cells were washed and surface stained for 20 minutes at 4 °C with the following antibodies: BV510-conjugated anti-human CD3 (Miltenyi, clone: BW264/56), APC-conjugated anti-human CD134 (OX40) (BD Pharmigen, clone: ACT35), APC-H7-conjugated anti-human CD4 (BD Pharmigen, clone: RPA-T4), PE-conjugated anti-human CD69 (Miltenyi, clone: FN50), PE-Cy 7-conjugated anti-human CD8 (BD Horizon, clone: RPA-T8).

Techniques: Flow Cytometry

Evaluation of CD4 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Percentage of (a, g) CD4 + , (b, h) CD154 + , (c, i) CD69 + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + cells in peripheral blood mononuclear cells (PBMCs) of (a, f) IFN- and (g, l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.

Journal: Frontiers in Immunology

Article Title: Multiple sclerosis patients under treatment with interferon β1-a or ocrelizumab exhibit different T and B cell responses to SARS-CoV-2 vaccine

doi: 10.3389/fimmu.2026.1773417

Figure Lengend Snippet: Evaluation of CD4 + cells in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Percentage of (a, g) CD4 + , (b, h) CD154 + , (c, i) CD69 + , (d, j) OX40 + , (e, k) TIGIT + , (f, l) CD62L + cells in peripheral blood mononuclear cells (PBMCs) of (a, f) IFN- and (g, l) OCRE-treated pwMS before (T0), 21 days after the first (T1) and the second (T2) vaccine dose. (a-f) IFN: T0: n=10; T1: n=10; T2: n= 10; (g-l) OCRE: T0: n=10; T1: n=10; T2: n= 9. Each data point represents a distinct individual (i.e., an independent biological sample). Data are presented as median values. Statistical analysis was performed by using the Wilcoxon signed-rank test (two tails); * p ≤ 0.05; ** p ≤ 0.01.

Article Snippet: After the stimulation, cells were washed and surface stained for 20 minutes at 4 °C with the following antibodies: BV510-conjugated anti-human CD3 (Miltenyi, clone: BW264/56), APC-conjugated anti-human CD134 (OX40) (BD Pharmigen, clone: ACT35), APC-H7-conjugated anti-human CD4 (BD Pharmigen, clone: RPA-T4), PE-conjugated anti-human CD69 (Miltenyi, clone: FN50), PE-Cy 7-conjugated anti-human CD8 (BD Horizon, clone: RPA-T8).

Techniques:

T cell comparison in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Fold change over basal [calculated as the ratio between the percentage of cells at T1 and T2 compared to baseline (T0)] of (a) CD8 + , (b) CD154 + , (c) CD69 + , (d) OX40 + , (e) TIGIT + , (f) CD62L + and (g) CD4 + , (h) CD154 + , (i) CD69 + , (j) OX40 + , (k) TIGIT + , (l) CD62L + cells in IFN (●) and OCRE (▲) -treated pwMS. Data are presented as median values. Statistical analysis was performed by using the Kruskal-Wallis test. * p ≤ 0.05, ** p ≤ 0.01.

Journal: Frontiers in Immunology

Article Title: Multiple sclerosis patients under treatment with interferon β1-a or ocrelizumab exhibit different T and B cell responses to SARS-CoV-2 vaccine

doi: 10.3389/fimmu.2026.1773417

Figure Lengend Snippet: T cell comparison in IFN- and OCRE-treated patients with multiple sclerosis (pwMS) undergoing BNT162b2 mRNA SARS-CoV-2 vaccination. Fold change over basal [calculated as the ratio between the percentage of cells at T1 and T2 compared to baseline (T0)] of (a) CD8 + , (b) CD154 + , (c) CD69 + , (d) OX40 + , (e) TIGIT + , (f) CD62L + and (g) CD4 + , (h) CD154 + , (i) CD69 + , (j) OX40 + , (k) TIGIT + , (l) CD62L + cells in IFN (●) and OCRE (▲) -treated pwMS. Data are presented as median values. Statistical analysis was performed by using the Kruskal-Wallis test. * p ≤ 0.05, ** p ≤ 0.01.

Article Snippet: After the stimulation, cells were washed and surface stained for 20 minutes at 4 °C with the following antibodies: BV510-conjugated anti-human CD3 (Miltenyi, clone: BW264/56), APC-conjugated anti-human CD134 (OX40) (BD Pharmigen, clone: ACT35), APC-H7-conjugated anti-human CD4 (BD Pharmigen, clone: RPA-T4), PE-conjugated anti-human CD69 (Miltenyi, clone: FN50), PE-Cy 7-conjugated anti-human CD8 (BD Horizon, clone: RPA-T8).

Techniques: Comparison

CD8 + and CD4 + T cell response in INF-treated patients with multiple sclerosis (pwMS) before and after BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis of spike-specific CD8 + and CD4 + T cells measured as the percentage of activated (a) CD69 + CD137 + and (d) CD154 + OX40 + T cells, respectively. Intracellular cytokines evaluation of (b) INF-γ and (c) TNF-α in CD8 + antigen-specific T cells and (e) IFN-γ, (f) TNF-α, and (g) IL-2 in CD4 + antigen-specific T cells. Analysis was performed after stimulation for 18 hours at 37 °C with a peptide pool spanning the entire Spike sequence. Data are presented as median values of at least n=4 subjects. Statistical analysis was performed by using the Mann-Whitney U -test (two tails); * p ≤ 0.05, ** p ≤ 0.01.

Journal: Frontiers in Immunology

Article Title: Multiple sclerosis patients under treatment with interferon β1-a or ocrelizumab exhibit different T and B cell responses to SARS-CoV-2 vaccine

doi: 10.3389/fimmu.2026.1773417

Figure Lengend Snippet: CD8 + and CD4 + T cell response in INF-treated patients with multiple sclerosis (pwMS) before and after BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis of spike-specific CD8 + and CD4 + T cells measured as the percentage of activated (a) CD69 + CD137 + and (d) CD154 + OX40 + T cells, respectively. Intracellular cytokines evaluation of (b) INF-γ and (c) TNF-α in CD8 + antigen-specific T cells and (e) IFN-γ, (f) TNF-α, and (g) IL-2 in CD4 + antigen-specific T cells. Analysis was performed after stimulation for 18 hours at 37 °C with a peptide pool spanning the entire Spike sequence. Data are presented as median values of at least n=4 subjects. Statistical analysis was performed by using the Mann-Whitney U -test (two tails); * p ≤ 0.05, ** p ≤ 0.01.

Article Snippet: After the stimulation, cells were washed and surface stained for 20 minutes at 4 °C with the following antibodies: BV510-conjugated anti-human CD3 (Miltenyi, clone: BW264/56), APC-conjugated anti-human CD134 (OX40) (BD Pharmigen, clone: ACT35), APC-H7-conjugated anti-human CD4 (BD Pharmigen, clone: RPA-T4), PE-conjugated anti-human CD69 (Miltenyi, clone: FN50), PE-Cy 7-conjugated anti-human CD8 (BD Horizon, clone: RPA-T8).

Techniques: Flow Cytometry, Sequencing, MANN-WHITNEY

CD8 + and CD4 + T cell response in OCRE-treated patients with multiple sclerosis (pwMS) before and after BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis of spike-specific CD8 + and CD4 + T cells measured as the percentage of activated (a) CD69 + CD137 + and (d) CD154 + OX40 + T cells, respectively. Intracellular cytokines evaluation of (b) IFN-γ and (c) TNF-α in CD8 + antigen-specific T cells and (e) IFN-γ, (f) TNF-α, and (g) IL-2 in CD4 + antigen-specific T cells. Analysis was performed after stimulation for 18 hours at 37 °C with a peptide pool spanning the entire Spike sequence. Data are presented as median values of at least n=3 subjects. Statistical analysis was performed by using the Mann-Whitney U -test (two tails); * p ≤ 0.05, ** p ≤ 0.01.

Journal: Frontiers in Immunology

Article Title: Multiple sclerosis patients under treatment with interferon β1-a or ocrelizumab exhibit different T and B cell responses to SARS-CoV-2 vaccine

doi: 10.3389/fimmu.2026.1773417

Figure Lengend Snippet: CD8 + and CD4 + T cell response in OCRE-treated patients with multiple sclerosis (pwMS) before and after BNT162b2 mRNA SARS-CoV-2 vaccination. Cumulative data of flow cytometry analysis of spike-specific CD8 + and CD4 + T cells measured as the percentage of activated (a) CD69 + CD137 + and (d) CD154 + OX40 + T cells, respectively. Intracellular cytokines evaluation of (b) IFN-γ and (c) TNF-α in CD8 + antigen-specific T cells and (e) IFN-γ, (f) TNF-α, and (g) IL-2 in CD4 + antigen-specific T cells. Analysis was performed after stimulation for 18 hours at 37 °C with a peptide pool spanning the entire Spike sequence. Data are presented as median values of at least n=3 subjects. Statistical analysis was performed by using the Mann-Whitney U -test (two tails); * p ≤ 0.05, ** p ≤ 0.01.

Article Snippet: After the stimulation, cells were washed and surface stained for 20 minutes at 4 °C with the following antibodies: BV510-conjugated anti-human CD3 (Miltenyi, clone: BW264/56), APC-conjugated anti-human CD134 (OX40) (BD Pharmigen, clone: ACT35), APC-H7-conjugated anti-human CD4 (BD Pharmigen, clone: RPA-T4), PE-conjugated anti-human CD69 (Miltenyi, clone: FN50), PE-Cy 7-conjugated anti-human CD8 (BD Horizon, clone: RPA-T8).

Techniques: Flow Cytometry, Sequencing, MANN-WHITNEY