Vaccination status and immune response to 13-valent pneumococcal conjugate vaccine in asplenic individuals

Vaccine ◽  
2015 ◽  
Vol 33 (14) ◽  
pp. 1688-1694 ◽  
Author(s):  
Per Nived ◽  
Charlotte Sværke Jørgensen ◽  
Bo Settergren
Vaccine ◽  
2017 ◽  
Vol 35 (29) ◽  
pp. 3639-3646 ◽  
Author(s):  
Per Nived ◽  
Johanna Nagel ◽  
Tore Saxne ◽  
Pierre Geborek ◽  
Göran Jönsson ◽  
...  

Vaccine ◽  
2013 ◽  
Vol 31 (42) ◽  
pp. 4765-4774 ◽  
Author(s):  
Gail L. Rodgers ◽  
Susanna Esposito ◽  
Nicola Principi ◽  
Maricruz Gutierrez-Brito ◽  
Javier Diez-Domingo ◽  
...  

Nutrients ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 4412
Author(s):  
Marcella Reale ◽  
Claudio Ucciferri ◽  
Erica Costantini ◽  
Marta Di Di Nicola ◽  
Annamaria Porreca ◽  
...  

Background: In people living with HIV, combination antiretroviral therapy (cART) reduces the risk of death, but the persistent immune-deficient state predisposes them to pneumococcal infections. Current guidelines encourage administering pneumococcal vaccine Prevenar 13 to patients living with HIV. Since probiotic supplementation could act as adjuvants and improve vaccine immunogenicity by modulating gut microbiota, the present study aimed to assess whether the effect of a formulation containing a combination of specific probiotics (Vivomixx®) could improve the immune response to 13-valent pneumococcal conjugate vaccine (PCV13) in adult people living with HIV. Methods: Thirty patients who were clinically stable and virologically suppressed, without opportunistic infections during this time and no ART changes in the 12 months before the study started were enrolled. Patients were divided into two groups: (1) received a placebo dose and (2) received Vivomixx® (1800 billion CFU) for four weeks before and after the vaccination with a single dose of PCV13. Results: Vivomixx® supplementation induced a better response to PCV13 immunization, as shown by greater change in anti-Pn CPS13 IgG and increase in salivary IgA, IL-10 and IL-8. Conclusions: Additional investigations will help to clearly and fully elucidate the optimal strains, doses, and timing of administration of probiotics to improve protection upon vaccination in immunocompromised individuals and the elderly.


2015 ◽  
Vol 213 (5) ◽  
pp. 848-855 ◽  
Author(s):  
Takayuki Hoshina ◽  
Shouichi Ohga ◽  
Junko Fujiyoshi ◽  
Etsuro Nanishi ◽  
Tomoko Takimoto ◽  
...  

Vaccine ◽  
2011 ◽  
Vol 29 (47) ◽  
pp. 8689-8695 ◽  
Author(s):  
Raquel Santamaria ◽  
Cibelly Goulart ◽  
Catia T. Perciani ◽  
Giovana C. Barazzone ◽  
Rimenys Jr. Carvalho ◽  
...  

2019 ◽  
Vol 6 (Supplement_2) ◽  
pp. S956-S957 ◽  
Author(s):  
Fernanda C Lessa ◽  
Michael Spiller ◽  
Xiyuan Wu ◽  
Rongrong Wang ◽  
Yoganand Chillarige ◽  
...  

Abstract Background Efficacy of 13-valent pneumococcal conjugate vaccine (PCV13) against pneumococcal pneumonia in adults aged >65 years was shown in a 2014 clinical trial. However, its benefits in countries with a mature PCV infant program remain unclear. In August 2014, PCV13 was recommended for all US adults aged >65 years. We evaluated the direct effect of this recommendation on pneumonia hospitalizations among the elderly. Methods We analyzed claims data from US Medicare beneficiaries aged >65 years enrolled in part A/B during September 1, 2014 through December 31, 2017. Participants were followed until they died, left part A/B, or developed a study outcome: community-acquired pneumonia (CAP), non-healthcare-associated CAP (non-HA CAP) or lobar pneumonia (LP). We identified outcomes using inpatient diagnosis codes, and vaccination status using procedure codes. We used discrete-time survival models, stratified by influenza season (October–April) and influenza vaccination status, to estimate incidence rate ratios (IRR) by pneumococcal vaccination status (PCV13-only vs. no pneumococcal vaccination). We adjusted for demographic factors, healthcare utilization, month/year of hospital discharge, and underlying conditions. We derived vaccine effectiveness (VE) and number of hospitalizations averted by PCV13 from the IRRs. Results Of 26.6 million beneficiaries in September 2014, 43.4% were male, 54.2% were aged 65–74 years, and 28.9% had a Charlson comorbidity score >3. PCV13 coverage increased from 0.8% in September 2014 to 41.5% in December 2017. Annual incidence of CAP, non-HA CAP, and LP are shown in the figure. PCV13-vaccinated persons were more likely to be older, sicker, and have received flu vaccine than unvaccinated persons. VE estimates for CAP, non-HA CAP, and LP ranged from 6.0–11.4%, 5.0–11.0%, and 1.3–11.0%, respectively. From September 2014 to December 2017, an estimated 28,600 (95% CI: 21,000–36,000) CAP, 18,700 (12,000–25,800) non-HA CAP and 1,100 (190–1,900) LP hospitalizations were averted. Conclusion Within 40 months after implementation of the adult PCV13 program, 2.0% (28,600) of US CAP hospitalizations were averted. Despite PCV13 effectiveness against adult CAP, only a small fraction of CAP hospitalizations was prevented. Disclosures All authors: No reported disclosures.


2013 ◽  
Vol 32 (11) ◽  
pp. 1180-1184 ◽  
Author(s):  
Katharina L. van Santen ◽  
Robert A. Bednarczyk ◽  
Dzifa Adjaye-Gbewonyo ◽  
Walter A. Orenstein ◽  
Robert Davis ◽  
...  

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