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Journal ArticleDOI

Cold-Recombinant Influenza A/California/10/78 (H1N1) Virus Vaccine (CR-37) in Seronegative Children: Infectivity and Efficacy Against Investigational Challenge

Robert B. Belshe, +1 more
- 01 May 1984 - 
- Vol. 149, Iss: 5, pp 735-740
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TLDR
Seronegative children inoculated intranasally with influenza A/California/10/78 (H1N1) cold-recombinant vaccine (CR-37) conferred significant protection from challenge with a high dose of CR-37.
Abstract
Forty-seven seronegative children were inoculated intranasally with influenza A/California/10/78 (H1N1) cold-recombinant vaccine (CR-37). Doses ranged from 10(3.2) to 10(7.2) TCID50 per child. The dose necessary to infect 50% of children (one HID50 ) was approximately 10(3.5) TCID50. Only two of eight children given 10(3.2) TCID50 became infected, and neither shed virus. The majority of children who were given 10(4.2), 10(5.2), 10(6.2), or 10(7.2) TCID50 of CR-37 became infected. Twenty-four of 39 children given greater than one HID50 of CR-37 shed vaccine virus. Overall, 31 of 39 became infected, as indicated by shedding of virus or antibody response or both. Although virus was shed for up to 12 days postinoculation, shedding of revertant virus was not detected. Six months after primary vaccination 26 children were challenged intranasally with 10(6.2) TCID50 of CR-37. Of 21 children previously infected with CR-37, only eight had further antibody increase, and none shed vaccine virus. In contrast, five of five (P less than .05) children not infected with CR-37 at the time of initial inoculation were infected with the challenge inoculum (as indicated by a fourfold rise in antibody titer) and three of five children shed vaccine virus. Previous infection with CR-37 conferred significant protection from challenge with a high dose of CR-37.

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The immune response to influenza infection.

TL;DR: There has been a great increase in knowledge of the different classes of lymphocytes, particularly T cells, and to a lesser extent of other cell types involved in the immune response to this virus.
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Development and persistence of local and systemic antibody responses in adults given live attenuated or inactivated influenza A virus vaccine.

TL;DR: The finding that live virus vaccine induced relatively long-lasting antibody in both local and serum compartments suggested that this vaccine may be a suitable alternative to inactivated vaccine for use in healthy persons.
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Immunity to Influenza A Virus Infection in Young Children: A Comparison of Natural Infection, Live Cold-Adapted Vaccine, and Inactivated Vaccine

TL;DR: Prechallenge nasal IgA, detected almost exclusively in subjects naturally infected or vaccinated with live ca virus, was associated with protection and inactivated vaccine failed to produce significant local IgA during the primary response, but seemed to prime for secondary local antibody responses after challenge with liveca virus.
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Four viral genes independently contribute to attenuation of live influenza A/Ann Arbor/6/60 (H2N2) cold-adapted reassortant virus vaccines.

TL;DR: The finding that four genes of the ca donor virus contribute to the att phenotype provides a partial explanation for the observed phenotypic stability of ca reassortant viruses following replication in humans.
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Identification of sequence changes in the cold-adapted, live attenuated influenza vaccine strain, A/Ann Arbor/6/60 (H2N2).

TL;DR: In this article, RNA segments encoding the PB2, P131, PA, NP, M1, M2, NS1, and NS2 proteins of the influenza A/Ann Arbor/6/60 (H2N2) wild-type (wt) virus and its cold-adapted (ca) derivative that has been used for preparing investigational live attenuated vaccines were obtained.
References
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Journal ArticleDOI

Adaptation and Growth Characteristics of Influenza Virus at 25° C

TL;DR: This work has shown that a relationship has been observed between virulence and the ability to grow at lower temperatures, and this has been used in the selection of attenuated variants.
Journal ArticleDOI

Hemagglutinin-specific enzyme-linked immunosorbent assay for antibodies to influenza A and B viruses.

TL;DR: The ELISA was more sensitive than the hemagglutination-inhibition assay, and the range of antibody titers measurable by ELISA in human serum was from less than 1:20 for children who had never experienced influenza infection to 1:400,000 for adults convalescing from a secondary infection.
Journal ArticleDOI

Dose response of A/Alaska/6/77 (H3N2) cold-adapted reassortant vaccine virus in adult volunteers: role of local antibody in resistance to infection with vaccine virus.

TL;DR: The failure of the vaccine virus to infect some volunteers was correlated with the presence of pre-inoculation nasal wash immunoglobulin A hemagglutinin antibody, indicating that the vaccine retains some mild reactogenicity at a high dosage.
Journal ArticleDOI

Evaluation of a Cold-Recombinant Influenza Virus Vaccine in Ferrets

TL;DR: Cold-recombinant strains of influenza virus were derived at 25 C using an attenuated cold-adapted and temperature-sensitive (ts) A/Ann Arbor/6/60 (H2N2) strain and wild-type (wt) strains of epidemic relevance to characterize the cold recombinants in ferrets.
Journal ArticleDOI

Cold-Adapted Recombinant Influenza A Virus Vaccines in Seronegative Young Children

TL;DR: Two live, attenuated, intranasally administered influenza virus vaccines were evaluated in 21 seronegative young children at Vanderbilt Children's Hospital and children previously vaccinated with the related strain, influenza A/Alaska (H3N2) virus, were significantly protected as judged by serologic evidence of reinfection.
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