Evidence map›Paper›PMID 28806922›Full record

ArticleBMC infectious diseases2017

Hepatitis B reactivation characterized by HBsAg negativity and anti-HbsAg antibodies persistence in haematopoietic stem cell transplanted patient after lamivudine withdrawal.

C Cerva, G Maffongelli, V Svicher, R Salpini, L Colagrossi, A Battisti, B Mariotti, R Cerretti, L Cudillo, L Sarmati

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

C CervaClinical Infectious Disease, Department of Systems Medicine, Tor Vergata University, Rome, Italy.
G MaffongelliClinical Infectious Disease, Department of Systems Medicine, Tor Vergata University, Rome, Italy. maffongelligaetano@gmail.com.
V SvicherDepartment of Experimental Medicine and Surgery, Tor Vergata University, Rome, Italy.
R SalpiniDepartment of Experimental Medicine and Surgery, Tor Vergata University, Rome, Italy.
L ColagrossiDepartment of Experimental Medicine and Surgery, Tor Vergata University, Rome, Italy.
A BattistiDepartment of Experimental Medicine and Surgery, Tor Vergata University, Rome, Italy.
B MariottiDepartment of Hematology, Stem Cell Transplant Unit, Tor Vergata University, Rome, Italy.
R CerrettiDepartment of Hematology, Stem Cell Transplant Unit, Tor Vergata University, Rome, Italy.
L CudilloDepartment of Hematology, Stem Cell Transplant Unit, Tor Vergata University, Rome, Italy.
L SarmatiClinical Infectious Disease, Department of Systems Medicine, Tor Vergata University, Rome, Italy.
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHBV reactivation is associated with high mortality rates in hematopoietic stem cell transplantation (HSCT) and prophylactic lamivudine (LMV) treatment is suggested to prevent this phenomenon. However, the duration of LMV treatment in HSCT patients is not fully defined and the time of immune recovery is considered the best parameter for a drug to be safely interrupted. In patients undergoing allogeneic HSCT, the time of immune recovery is not easy to define and may take years after transplantation and prolonged LMV treatments, which can lead to drug-resistant viral strains. CASE PRESENTATION: An anti-HBc-positive hematological patient who was undergoing prolonged immunosuppression and who experienced HBV reactivation 3 months after the suspension of a prolonged LMV prophylaxis is described. HBV-DNA matching an atypical serological profile characterized by HbsAg negativity and anti-HBs positivity was detected in the patient. The genotypic analysis of the HBV strain identified T127P, F170FL and S204R mutations of HbsAg, which can hinder HBsAg recognition in a diagnostic assay.

conclusionsHBV reactivation in the HSCT host can be sustained by HBsAg viral variants with characteristics of altered immunogenicity that cannot be detected by usual laboratory tests. This clinical case description suggests the importance of screening for serum HBV-DNA levels in the diagnosis of HBV reactivation and monitoring HBV-DNA after prophylaxis suspension, particularly in HSCT subjects who have undergone prolonged periods of LMV treatment.

Indexed as

Antibiotic ProphylaxisHematopoietic Stem Cell TransplantationHepatitis BHepatitis B AntibodiesHepatitis B Surface AntigensHepatitis B virusHumansImmunocompromised HostLamivudineMaleMiddle AgedVirus ActivationHepatitis B AntibodiesHepatitis B Surface AntigensLamivudineHbv DNAHBV reactivationHematopoietic stem cell transplantationHepatitis BProphylaxis

Identifiers

PMID28806922
PMCPMC5557326
OpenAlexW2745697709

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LicenceCC BY
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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.