Evidence map›Paper›PMID 42498816›Full record

ArticleScientific reports2026

Invasive pneumococcal disease unmasks monoclonal immunoglobulins and antibody deficiencies: a multicenter prospective study in adults.

Tor Härnqvist, Karin Bergman, Åsa Mellgren, Magnus Brink, Amanda Nilsson, Staffan Nilsson, Bengt Andersson, Rune Andersson, Anna Lundgren, Johanna Karlsson and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2026. 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
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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.

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

11 authors.

Tor Härnqvist *Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden. tor.harnqvist@gu.se.ORCID 0000-0002-1178-6577
Karin Bergman *Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden.
Åsa MellgrenDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden.
Magnus BrinkDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden.
Amanda NilssonDepartment of Infectious Diseases, NU Hospital Group, Trollhättan, Region Västra Götaland, Sweden.
Staffan NilssonDepartment of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Bengt AnderssonDepartment of Clinical Immunology and Transfusion Medicine, Sahlgrenska University Hospital, Gothenburg, Region Västra Götaland, Sweden.
Rune AnderssonDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden.
Anna LundgrenDepartment of Clinical Immunology and Transfusion Medicine, Sahlgrenska University Hospital, Gothenburg, Region Västra Götaland, Sweden.
Johanna KarlssonDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden.
Susann SkovbjergDepartment of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, SE-413 46, Gothenburg, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunoglobulins (Ig) are essential for protection against invading pneumococci but are not routinely analyzed in patients with invasive pneumococcal disease (IPD). In this prospective study, we assessed the prevalence of monoclonal Ig (M protein) and analyzed Ig concentrations in sera from 156 adult IPD patients (median age 70 years). Patients were sampled during acute infection (n = 153) and in the convalescence phase 2-4 months after acute infection (n = 76). Sixty-four sex- and age-matched individuals without IPD served as controls. During infection, M protein was detected in 22% (31/141) of patients without previously known hematological malignancy as compared with 5% of the controls (p = 0.002). Seven of these patients were subsequently diagnosed with a hematological malignancy, including multiple myeloma, Waldenstrom macroglobulinemia, and mantle cell lymphoma. Another 12 patients were diagnosed with monoclonal gammopathy of undetermined significance (MGUS). Convalescence levels of IgA, IgG2, or IgG4 were below the reference intervals in 16-20% of patients and 0-2% of controls. Three patients were diagnosed with a primary Ig deficiency, and seven patients started Ig replacement therapy. Our findings suggest that assessment of M protein and Ig levels could be considered in adults with IPD, as an episode of IPD may unmask a previously undiagnosed B-cell malignancy or immunodeficiency.

Indexed as

Antibodies, MonoclonalPneumococcal InfectionsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedMultiple MyelomaProspective StudiesStreptococcus pneumoniaeAntibodies, MonoclonalHypogammaglobulinemiaImmune deficiencyImmunoglobulinInvasive pneumococcal diseaseMonoclonal gammopathy of undetermined significanceM proteinMultiple myeloma

Identifiers

PMID42498816
PMCPMC13400745

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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.