This is a Phase I, randomized controlled trial to evaluate the safety of Lactobacillus rhamnosus GG (LGG) versus placebo in elderly subjects receiving the live attenuated influenza vaccine. Lactobacilli are part of the normal flora of the intestine. LGG is one of several strains of Lactobacilli that is used as a probiotic or microorganism administered to confer "health benefits". Our research is focused on studying the possible therapeutic effects of LGG. The study hypotheses are: 1. LGG or placebo administered twice daily will be safe and well tolerated in elderly subjects who have just received the live attenuated influenza vaccine, 2. The immune response to the influenza vaccine at day 21, 28, and 56 will be higher in the LGG group than the placebo group, 3. The diversity of the microbiota in nasopharyngeal and stool specimens at day 21, 28, and 56 will be greater in the LGG group than the placebo group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
QUADRUPLE
Enrollment
30
Study drug capsules (1x10\^10 LGG/capsule) are to be taken orally twice a day every day on an outpatient basis for 28 days
Placebo capsules composed of microcrystalline cellulose are to be taken orally twice a day on an outpatient basis for 28 days.
0.2 mL pre-filled, single use intranasal spray
Massachusetts General Hospital
Boston, Massachusetts, United States
Occurrence of adverse events that are possibly or probably related to administration of LGG
Adverse events will be detected during study visits with standardized questionnaires, medical history, vital signs, physical examinations, laboratory tests and review of subject diaries as well as between study visits on telephone calls based on responses to adverse event questionnaires. Additionally, subjects are encouraged to call the PI or study staff at any time if they are experiencing an adverse event.
Time frame: Subjects will be followed from the study start through the end of the 2012-2013 influenza season (as defined by CDC) with an anticipated average for most subjects of 13 months
Anti-influenza systemic immune response (HAI, MN titers and IgA titers)
HAI, MN titers and IgA titers will be measured at baseline and on days 21, 28, 56 post LAIV vaccination
Time frame: Baseline through day 56 post LAIV vaccination
Anti influenza mucosal immune response (IgA titers)
IgA levels will be measured at baseline, and days 21, 28 and 56 post LAIV immunization
Time frame: Baseline through day 56 post LAIV vaccination
Richness and microbial diversity in nasopharyngeal and stool specimens
Measure of the richness and microbial diversity in nasopharyngeal and stool specimens using pyrosequencing
Time frame: Baseline through day 56 post LAIV vaccination
Anti influenza systemic immune response post TIV vaccination
Anti influenza systemic immune response (HAI and MN titers) will be measured before and 28 days after TIV immunization in the fall 2012.
Time frame: Fall 2012 - prior to and 28 days post TIV vaccination
Occurence of influenza-like illness during 2012-2013 influenza season
Subjects will telephoned every month after receiving the TIV vaccination in the fall of 2012, through the end of the 2012-2013 influenza season, to determine if they have an influenza-like illness. They will also be asked to keep a study diary if they experience any influenza-like symptoms
Time frame: Baseline through the end of the 2012-2013 influenza season (anticipated average of 13 months)
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