Evidence map›Paper›PMID 42681404›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2026

The Immunology of Transfusion Medicine: Past, Present, and Future.

Connie M Arthur, Sean R Stowell

Abstract readReview
PubMed Publisher
In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 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
–field-weighted citation impact
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

2 authors.

Connie M ArthurDivision of Transfusion Medicine, Mass General Brigham, Harvard Medical School, Boston, MA, USA. cmarthur@bwh.harvard.edu.
Sean R StowellDivision of Transfusion Medicine, Mass General Brigham, Harvard Medical School, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of alloantigens has been central to understanding how polymorphic variation influences transfusion safety through potential immune incompatibilities between individuals. Patients may possess naturally occurring antibodies that develop within the first few months of life or form alloantibodies after exposure to alloantigens during transfusion or pregnancy. These antibodies complicate the search for compatible blood and increase the risk of hemolytic disease of the fetus and newborn, as well as fetal and neonatal thrombocytopenia. Alloimmune mechanisms can also contribute to transfusion-related acute lung injury and transfusion-associated graft-versus-host disease. Beyond the direct complications of alloimmunity, changes in the metabolic and immunologic characteristics of transfused blood products can affect recipient immune function. In this review, we explore the historical interplay between immunology and transfusion medicine and highlight emerging preclinical and clinical insights into the field, with particular focus on the development and clinical implications of red blood cell alloimmunization.

Indexed as

Transfusion MedicineTransfusion ReactionAnimalsBlood TransfusionErythrocytesFemaleGraft vs Host DiseaseHumansIsoantibodiesIsoantigensPregnancyTransfusion-Related Acute Lung InjuryIsoantibodiesIsoantigensBloodComplicationsExperimental approachesModelsToolsTransfusion

Identifiers

What Socratic 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 Socratic graph.