Abstract | BACKGROUND:
Abatacept acts as a co-stimulation modulator preventing activation of T cells. Although it is approved for the treatment of rheumatoid arthritis (RA), its effects on adaptive immune response have not been fully elucidated. OBJECTIVES: METHODS: RESULTS: Total immunoglobulin serum levels significantly decreased after 3 months of treatment and correlated positively with disease activity both at baseline and after 3 months of abatacept treatment. A reduction of serum IgM, IgG, IgA and RF was also demonstrated. The absolute number and percentage of cytotoxic (CD8+) T cells significantly decreased after 3 months of abatacept treatment, in particular the percentage of cytotoxic (CD8+) T cells significantly decreased only in patients responding to the treatment. CONCLUSIONS: Our results highlight a different role of abatacept in the modulation of the adaptive immune response in RA by the reduction of polyclonal B-cell activation and cytotoxic T cells.
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Authors | Paola Conigliaro, Paola Triggianese, Emiliano Giampà, Maria S Chimenti, Barbara Kroegler, Roberto Perricone |
Journal | The Israel Medical Association journal : IMAJ
(Isr Med Assoc J)
Vol. 19
Issue 7
Pg. 406-410
(07 2017)
ISSN: 1565-1088 [Print] Israel |
PMID | 28786253
(Publication Type: Journal Article)
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Chemical References |
- Antirheumatic Agents
- Autoantibodies
- Immunoglobulin A
- Immunoglobulin G
- Immunoglobulin M
- Abatacept
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Topics |
- Abatacept
(pharmacology)
- Antirheumatic Agents
(pharmacology)
- Arthritis, Rheumatoid
(blood, drug therapy, immunology)
- Autoantibodies
(blood)
- B-Lymphocytes
(drug effects)
- Cohort Studies
- Humans
- Immunoglobulin A
(blood)
- Immunoglobulin G
(blood)
- Immunoglobulin M
(blood)
- T-Lymphocyte Subsets
(drug effects)
- T-Lymphocytes, Cytotoxic
(drug effects)
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