Evidence map›Paper›PMID 23249609›Full record

ArticleHuman vaccines & immunotherapeutics2013

Novel therapeutic vaccines [(HSP65 + IL-12)DNA-, granulysin- and Ksp37-vaccine] against tuberculosis and synergistic effects in the combination with chemotherapy.

Yoko Kita, Satomi Hashimoto, Toshihiro Nakajima, Hitoshi Nakatani, Shiho Nishimatsu, Yasuko Nishida, Noriko Kanamaru, Yasuhumi Kaneda, Yasushi Takamori, David McMurray and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. CTLs: Killers of intracellular bacteria.Frontiers in cellular and infection microbiology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 3 countries.

Yoko KitaClinical Research Center; National Hospital Organization Kinki-chuo Chest Medical Center; Kitaku, Sakai Japan.
Satomi Hashimoto
Toshihiro Nakajima
Hitoshi Nakatani
Shiho Nishimatsu
Yasuko Nishida
Noriko Kanamaru
Yasuhumi Kaneda
Yasushi Takamori
David McMurray
Esterlina V Tan
Marjorie L Cang
Paul Saunderson
E C Dela Cruz
Masaji Okada
National Kinki Chuo Hospital for Chest Disease · JPClinical Research Management · USCollege Station Medical Center · USIkeda Municipal Hospital · JPOsaka University · JPTsurumi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMulti-drug resistant tuberculosis (MDR-TB) and extremely drug resistant (XDR) TB are big problems in the world. We have developed novel TB therapeutic vaccines, HVJ-Envelope/HSP65 + IL-12 DNA vaccine (HSP65-vaccine), granulysin vaccine and killer specific secretory protein of 37kDa (Ksp37) vaccine. METHODS AND

resultsHSP65 vaccine showed strong therapeutic effect against both MDR-TB and XDR-TB in mice. Intradermal immunization of HSP65-vaccine showed stronger therapeutic effect against TB than intramuscular or subcutaneous immunization. Furthermore, the synergistic therapeutic effect was observed when the vaccine was administrated in combination with Isoniazid (INH), which is a first line drug for chemotherapy. The combination of types of vaccines (HSP65- and granulysin- vaccines) also showed synergistic therapeutic effect. In the monkey model, granulysin-vaccine prolonged the survival period after the infection of TB and long-term survival was observed in vaccine-treated group. We examined the potential of two kinds of novel DNA vaccines (Ksp37-vaccine and granulysin-vaccine). Both vaccines augmented in vivo differentiation of CTL against TB. We measured the amount of Ksp37 protein in human serum and revealed that the level of Ksp37 protein of patients with tuberculosis was lower than that of healthy volunteers. Therefore, we established Ksp37 transgenic mice as well as granulysin transgenic mice to elucidate the function of those proteins. Both transgenic mice were resistant to TB infection.

conclusionThese data indicate the potential of combinational therapy; the combination of two DNA vaccines or combination of DNA vaccine with antibiotic drug. Thus, it will provide a novel strategy for the treatment of MDR-TB.

Indexed as

AnimalsAntigens, Differentiation, T-LymphocyteAntitubercular AgentsBacterial ProteinsBlood ProteinsChaperonin 60Combined Modality TherapyDisease Models, AnimalInterleukin-12Macaca fascicularisMice, TransgenicMycobacterium tuberculosisT-Lymphocytes, CytotoxicTreatment OutcomeTuberculosisTuberculosis VaccinesAntigens, Differentiation, T-LymphocyteAntitubercular AgentsBacterial ProteinsBlood ProteinsChaperonin 60FGFBP2 protein, humanGNLY protein, humanheat-shock protein 65, MycobacteriumInterleukin-12Tuberculosis VaccinesVaccines, DNAchemotherapygranulysin vaccineHSP65 DNA + IL-12 DNA vaccineKsp37 transgenic mouseKsp37 vaccineMDR-TBsynergistic therapeutic efficacytherapeutic vaccine againstXDR-TB

Identifiers

PMID23249609
PMCPMC3891708
OpenAlexW2046267905

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.