Serum IgG2 levels predict long-term protection following pneumococcal vaccination in systemic lupus erythematosus (SLE)

Vaccine ◽  
2020 ◽  
Vol 38 (44) ◽  
pp. 6859-6863
Author(s):  
Anne-Laure Gerard ◽  
Tiphaine Goulenok ◽  
Mathilde Bahuaud ◽  
Chrystelle Francois ◽  
Pierre Aucouturier ◽  
...  
2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 360.3-360
Author(s):  
T. Goulenok ◽  
A. L. Gerard ◽  
M. Bahuaud ◽  
P. Aucouturier ◽  
H. Moins ◽  
...  

Background:Systemic lupus erythematosus (SLE) patients are at increased risk forStreptococcus pneumoniaeinfection. Although pneumococcal vaccination is an attractive method to prevent invasive pneumococcal infection, vaccination coverage remains dramatically low in SLE. Moreover, the efficacy of vaccination may be reduced in SLE patients and sequential pneumococcal vaccination using new conjugated pneumococcal vaccines in combination with 23-valent pneumococcal polysaccharide vaccine (PPV23) is now advocated. However, limited study directly addressed the immune efficacy of such prime-and-boost strategy in SLEObjectives:We aimed to measure the immunological efficacy of the sequential pneumococcal vaccination using PCV13 in combination with PPV23 and identify factors associated with long-term immune protection following vaccination in SLE.Methods:SLE patients received PCV13 vaccine followed by PPSV23 vaccine 8 weeks later. Immune protection, defined by an antigen-specific IgG concentration ≥ 1.3 µg/mL for at least 70% of 7 pneumococcal serotypes (4, 6B, 9V, 14, 18C, 19F, 23F), was assessed at baseline, 2 months, 12 months, and 36 months, defining very long-term protection.Results:21 (40[25-75] years; 85.7% female) SLE patients received the sequential PCV13/PPV23 vaccines. Only 10 (47.6%) showed a sustained immune protection against pneumococcal infection 36 months after PCV13 shot (very long-term protected, VLTP). Eleven patients had no long-term protection (NLTP) with a seroconversion that never (n=6) or only transiently (n=5) occurred. SLE disease features, treatment received and immunological characteristic did not differ between VLTP and NLTP patients except for a lower serum IgG2 levels in NLTP (1.45 [1.30, 1.82] vs 3.30 [2.92, 4.44] g/L, p<0.001). Noteworthy the ROC curve showed that the serum IgG2 level before vaccination (AUC 0.95 [95% CI: 0.84-1]; p=0.004) was predictive for very long-term protection. A baseline serum IgG2 level of 2.125µg/ml or more showed a sensitivity of 100% and a specificity of 90.9% for very long-term protectionConclusion:The benefit of sequential PCV13/PPV23 vaccination in SLE is limited. Baseline IgG2 serum level before vaccination is strongly indicative of very long term protection following vaccinationDisclosure of Interests:None declared


1975 ◽  
Vol 37 (6) ◽  
pp. 924-929 ◽  
Author(s):  
Hideaki YAMAURA ◽  
Masaharu RIKIMARU ◽  
Isamu TAKAHASHI ◽  
Sadao ANAN ◽  
Tomio AKIYAMA ◽  
...  

Lupus ◽  
1998 ◽  
Vol 7 (2) ◽  
pp. 80-85 ◽  
Author(s):  
◽  
E Tsakonas ◽  
L Joseph ◽  
J M Esdaile ◽  
D Choquette ◽  
...  

2019 ◽  
Author(s):  
Kyriakos A. Kirou ◽  
Michael D. Lockshin

Systemic lupus erythematosus (SLE) is a chronic systemic autoimmune illness characterized by autoantibodies directed at nuclear antigens that cause clinical and laboratory abnormalities, such as rash, arthritis, leukopenia and thrombocytopenia, alopecia, fever, nephritis, and neurologic disease. Most or all of the symptoms of acute lupus are attributable to immunologic attack on the affected organs. Many complications of long-term disease are attributable to both the disease and its treatment. Intense sun exposure, drug reactions, and infections are circumstances that induce flare; the aim of treatment is to induce remission. This chapter is divided into sections dealing with SLE’s definitions; epidemiology; pathogenesis; disease classification, diagnosis, and differential diagnosis; and treatment. This review contains 10 figures, 12 tables, and 97 references. Key Words: Systemic lupus erythematosus, Dermatomyositis, Sjögren syndrome, rheumatoid arthritis, systemic sclerosis, Discoid lupus erythematosus, truncal psoriasiform, annular polycyclic rash


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