Evidence map›Paper›PMID 38186001›Full record

ArticleJournal of biosciences2024

Epidemiology: Gray immunity model gives qualitatively different predictions.

Milind Watve, Himanshu Bhisikar, Rohini Kharate, Srashti Bajpai

Open access · hybridAbstract read
PubMed
In one paragraph

Article in Journal of biosciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 100% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 3 institutions in 1 country.

Milind WatveIndependent Researcher, Pune 411 052, India.
Himanshu Bhisikar
Rohini Kharate
Srashti Bajpai
Indian Institute of Science Education and Research Pune · INMIT World Peace University · INUnit for Research and Development of Information Products · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compartmental models that dynamically divide the host population into categories such as susceptible, infected, and immune constitute the mainstream of epidemiological modelling. Effectively, such models treat infection and immunity as binary variables. We constructed an individual-based stochastic model that considers immunity as a continuous variable and incorporates factors that bring about small changes in immunity. The small immunity effects (SIE) comprise cross-immunity by other infections, small increments in immunity by subclinical exposures, and slow decay in the absence of repeated exposure. The model makes qualitatively different epidemiological predictions, including repeated waves without the need for new variants, dwarf peaks (peak and decline of a wave much before reaching herd immunity threshold), symmetry in upward and downward slopes of a wave, endemic state, new surges after variable and unpredictable gaps, and new surges after vaccinating majority of the population. In effect, the SIE model raises alternative possible causes of universally observed dwarf and symmetric peaks and repeated surges, observed particularly well during the COVID-19 pandemic. We also suggest testable predictions to differentiate between the alternative causes for repeated waves. The model further shows complex interactions of different interventions that can be synergistic as well as antagonistic. It also suggests that interventions that are beneficial in the short run could also be hazardous in the long run.

Indexed as

COVID-19PandemicsHumansImmunity

Identifiers

PMID38186001
OpenAlexW4390618887

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.