Titre : Immunoprotéines

Immunoprotéines : Questions médicales fréquentes

Questions fréquentes et termes MeSH associés

Diagnostic 5

#1

Comment diagnostiquer une carence en immunoprotéines ?

Des tests sanguins mesurant les niveaux d'immunoglobulines sont effectués.
Immunoglobulines Tests de laboratoire
#2

Quels tests sont utilisés pour évaluer les immunoprotéines ?

Les tests d'électrophorèse des protéines et les dosages d'anticorps sont courants.
Électrophorèse Anticorps
#3

Les biopsies sont-elles nécessaires pour le diagnostic ?

Elles peuvent être nécessaires pour évaluer des maladies sous-jacentes affectant les immunoprotéines.
Biopsie Maladies auto-immunes
#4

Quels symptômes indiquent un problème d'immunoprotéines ?

Infections fréquentes, fatigue chronique et retard de guérison peuvent indiquer un problème.
Infections Fatigue
#5

Peut-on diagnostiquer des troubles immunitaires par imagerie ?

L'imagerie peut aider à détecter des anomalies, mais les tests sanguins sont plus précis.
Imagerie médicale Troubles immunitaires

Symptômes 5

#1

Quels sont les symptômes d'une déficience en immunoprotéines ?

Infections récurrentes, inflammation, et fatigue sont des symptômes courants.
Déficience immunitaire Inflammation
#2

Les allergies sont-elles liées aux immunoprotéines ?

Oui, les allergies impliquent une réponse immunitaire anormale, souvent médiée par des immunoprotéines.
Allergies Réponse immunitaire
#3

Comment les maladies auto-immunes affectent-elles les immunoprotéines ?

Elles peuvent entraîner une production excessive ou insuffisante d'immunoprotéines.
Maladies auto-immunes Immunoprotéines
#4

Les symptômes varient-ils selon le type d'immunoprotéines ?

Oui, différents types d'immunoprotéines peuvent causer des symptômes variés.
Types d'immunoprotéines Symptômes
#5

Les infections chroniques sont-elles un signe d'immunoprotéines faibles ?

Oui, des infections fréquentes peuvent indiquer une faiblesse du système immunitaire.
Infections chroniques Système immunitaire

Prévention 5

#1

Comment prévenir les infections chez les patients immunodéprimés ?

Il est crucial de maintenir une bonne hygiène, éviter les foules et se faire vacciner.
Prévention des infections Hygiène
#2

Les changements de mode de vie aident-ils à renforcer l'immunité ?

Oui, une alimentation équilibrée, l'exercice et le sommeil améliorent la santé immunitaire.
Mode de vie Santé immunitaire
#3

Les suppléments nutritionnels sont-ils bénéfiques ?

Certains suppléments, comme la vitamine D, peuvent soutenir le système immunitaire.
Suppléments nutritionnels Vitamine D
#4

Les consultations régulières sont-elles importantes ?

Oui, des suivis réguliers permettent d'ajuster les traitements et de surveiller l'état de santé.
Consultations médicales Suivi médical
#5

Les pratiques de vaccination sont-elles essentielles ?

Oui, elles sont cruciales pour prévenir les infections chez les personnes à risque.
Vaccination Prévention des infections

Traitements 5

#1

Quels traitements existent pour les troubles des immunoprotéines ?

Les traitements incluent des immunoglobulines intraveineuses et des thérapies immunosuppressives.
Immunoglobulines Thérapies immunosuppressives
#2

Les vaccins sont-ils efficaces pour les personnes avec des troubles immunitaires ?

Les vaccins peuvent être moins efficaces, mais ils sont souvent recommandés pour prévenir les infections.
Vaccins Prévention des infections
#3

Comment les thérapies géniques aident-elles les déficiences immunitaires ?

Elles visent à corriger les anomalies génétiques responsables des troubles immunitaires.
Thérapie génique Déficiences immunitaires
#4

Les traitements sont-ils personnalisés selon le patient ?

Oui, les traitements sont souvent adaptés en fonction des besoins spécifiques du patient.
Médecine personnalisée Traitements
#5

Les médicaments immunosuppresseurs sont-ils risqués ?

Oui, ils augmentent le risque d'infections et nécessitent une surveillance étroite.
Médicaments immunosuppresseurs Surveillance médicale

Complications 5

#1

Quelles complications peuvent survenir avec des troubles immunitaires ?

Les complications incluent des infections graves, des cancers et des maladies auto-immunes.
Infections graves Cancers
#2

Les troubles des immunoprotéines augmentent-ils le risque de cancer ?

Oui, certaines déficiences immunitaires sont associées à un risque accru de cancers.
Risque de cancer Déficiences immunitaires
#3

Comment les infections opportunistes affectent-elles les patients ?

Elles peuvent causer des maladies graves chez les patients immunodéprimés.
Infections opportunistes Immunodéprimés
#4

Les complications peuvent-elles être évitées ?

Certaines complications peuvent être évitées par une surveillance et un traitement appropriés.
Surveillance médicale Traitement
#5

Les maladies auto-immunes sont-elles une complication fréquente ?

Oui, elles peuvent survenir en raison d'une réponse immunitaire inappropriée.
Maladies auto-immunes Réponse immunitaire

Facteurs de risque 5

#1

Quels facteurs augmentent le risque de troubles immunitaires ?

L'âge, les maladies chroniques, et les antécédents familiaux sont des facteurs de risque.
Âge Maladies chroniques
#2

Le stress a-t-il un impact sur le système immunitaire ?

Oui, le stress chronique peut affaiblir le système immunitaire et augmenter les risques.
Stress Système immunitaire
#3

Les infections antérieures influencent-elles le risque futur ?

Certaines infections peuvent affaiblir le système immunitaire, augmentant le risque futur.
Infections Système immunitaire
#4

L'alimentation joue-t-elle un rôle dans la santé immunitaire ?

Oui, une alimentation déséquilibrée peut affaiblir le système immunitaire.
Alimentation Santé immunitaire
#5

Les médicaments peuvent-ils affecter le système immunitaire ?

Oui, certains médicaments, comme les immunosuppresseurs, peuvent affaiblir l'immunité.
Médicaments Immunosuppresseurs
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"Question", "name": "Les changements de mode de vie aident-ils à renforcer l'immunité ?", "position": 12, "acceptedAnswer": { "@type": "Answer", "text": "Oui, une alimentation équilibrée, l'exercice et le sommeil améliorent la santé immunitaire." } }, { "@type": "Question", "name": "Les suppléments nutritionnels sont-ils bénéfiques ?", "position": 13, "acceptedAnswer": { "@type": "Answer", "text": "Certains suppléments, comme la vitamine D, peuvent soutenir le système immunitaire." } }, { "@type": "Question", "name": "Les consultations régulières sont-elles importantes ?", "position": 14, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des suivis réguliers permettent d'ajuster les traitements et de surveiller l'état de santé." } }, { "@type": "Question", "name": "Les pratiques de vaccination sont-elles essentielles ?", "position": 15, "acceptedAnswer": { "@type": "Answer", "text": "Oui, elles sont cruciales pour prévenir les infections chez les personnes à risque." } }, { "@type": "Question", "name": "Quels traitements existent pour les troubles des immunoprotéines ?", "position": 16, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements incluent des immunoglobulines intraveineuses et des thérapies immunosuppressives." } }, { "@type": "Question", "name": "Les vaccins sont-ils efficaces pour les personnes avec des troubles immunitaires ?", "position": 17, "acceptedAnswer": { "@type": "Answer", "text": "Les vaccins peuvent être moins efficaces, mais ils sont souvent recommandés pour prévenir les infections." } }, { "@type": "Question", "name": "Comment les thérapies géniques aident-elles les déficiences immunitaires ?", "position": 18, "acceptedAnswer": { "@type": "Answer", "text": "Elles visent à corriger les anomalies génétiques responsables des troubles immunitaires." } }, { "@type": "Question", "name": "Les traitements sont-ils personnalisés selon le patient ?", "position": 19, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les traitements sont souvent adaptés en fonction des besoins spécifiques du patient." } }, { "@type": "Question", "name": "Les médicaments immunosuppresseurs sont-ils risqués ?", "position": 20, "acceptedAnswer": { "@type": "Answer", "text": "Oui, ils augmentent le risque d'infections et nécessitent une surveillance étroite." } }, { "@type": "Question", "name": "Quelles complications peuvent survenir avec des troubles immunitaires ?", "position": 21, "acceptedAnswer": { "@type": "Answer", "text": "Les complications incluent des infections graves, des cancers et des maladies auto-immunes." } }, { "@type": "Question", "name": "Les troubles des immunoprotéines augmentent-ils le risque de cancer ?", "position": 22, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines déficiences immunitaires sont associées à un risque accru de cancers." } }, { "@type": "Question", "name": "Comment les infections opportunistes affectent-elles les patients ?", "position": 23, "acceptedAnswer": { "@type": "Answer", "text": "Elles peuvent causer des maladies graves chez les patients immunodéprimés." } }, { "@type": "Question", "name": "Les complications peuvent-elles être évitées ?", "position": 24, "acceptedAnswer": { "@type": "Answer", "text": "Certaines complications peuvent être évitées par une surveillance et un traitement appropriés." } }, { "@type": "Question", "name": "Les maladies auto-immunes sont-elles une complication fréquente ?", "position": 25, "acceptedAnswer": { "@type": "Answer", "text": "Oui, elles peuvent survenir en raison d'une réponse immunitaire inappropriée." } }, { "@type": "Question", "name": "Quels facteurs augmentent le risque de troubles immunitaires ?", "position": 26, "acceptedAnswer": { "@type": "Answer", "text": "L'âge, les maladies chroniques, et les antécédents familiaux sont des facteurs de risque." } }, { "@type": "Question", "name": "Le stress a-t-il un impact sur le système immunitaire ?", "position": 27, "acceptedAnswer": { "@type": "Answer", "text": "Oui, le stress chronique peut affaiblir le système immunitaire et augmenter les risques." } }, { "@type": "Question", "name": "Les infections antérieures influencent-elles le risque futur ?", "position": 28, "acceptedAnswer": { "@type": "Answer", "text": "Certaines infections peuvent affaiblir le système immunitaire, augmentant le risque futur." } }, { "@type": "Question", "name": "L'alimentation joue-t-elle un rôle dans la santé immunitaire ?", "position": 29, "acceptedAnswer": { "@type": "Answer", "text": "Oui, une alimentation déséquilibrée peut affaiblir le système immunitaire." } }, { "@type": "Question", "name": "Les médicaments peuvent-ils affecter le système immunitaire ?", "position": 30, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certains médicaments, comme les immunosuppresseurs, peuvent affaiblir l'immunité." } } ] } ] }
Dr Olivier Menir

Contenu validé par Dr Olivier Menir

Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale


Validation scientifique effectuée le 24/06/2026

Contenu vérifié selon les dernières recommandations médicales

Sous-catégories

47 au total
└─

Protéine C-réactive

C-Reactive Protein D002097 - D12.776.124.486.157
└─

Protéines du système du complément

Complement System Proteins D003165 - D12.776.124.486.274
└─

Protéines des granules de l'éosinophile

Eosinophil Granule Proteins D047091 - D12.776.124.486.379
└─

Opsonines

Opsonin Proteins D009895 - D12.776.124.486.657
└─└─

Anaphylatoxines

Anaphylatoxins D000706 - D12.776.124.486.274.024
└─└─

Enzymes activatrices du complément

Complement Activating Enzymes D003166 - D12.776.124.486.274.045
└─└─

Complément C1

Complement C1 D003172 - D12.776.124.486.274.050
└─└─

Complément C2

Complement C2 D003175 - D12.776.124.486.274.150
└─└─

Complément C3

Complement C3 D003176 - D12.776.124.486.274.250
└─└─

Complément C4

Complement C4 D003181 - D12.776.124.486.274.350
└─└─

Complément C5

Complement C5 D003182 - D12.776.124.486.274.450
└─└─

Complément C6

Complement C6 D003183 - D12.776.124.486.274.550
└─└─

Complément C7

Complement C7 D003184 - D12.776.124.486.274.650
└─└─

Complément C8

Complement C8 D003185 - D12.776.124.486.274.750
└─└─

Complément C9

Complement C9 D003186 - D12.776.124.486.274.850
└─└─

Protéines inhibitrices du complément

Complement Inactivator Proteins D003169 - D12.776.124.486.274.920
└─└─

Complexe d'attaque membranaire du complément

Complement Membrane Attack Complex D015938 - D12.776.124.486.274.930
└─└─

Protéine cationique de l'éosinophile

Eosinophil Cationic Protein D047150 - D12.776.124.486.379.249
└─└─

Neurotoxine dérivée des éosinophiles

Eosinophil-Derived Neurotoxin D047208 - D12.776.124.486.379.275
└─└─

Protéine basique majeure de l'éosinophile

Eosinophil Major Basic Protein D047093 - D12.776.124.486.379.500
└─└─

Eosinophil Peroxidase

Eosinophil Peroxidase D047209 - D12.776.124.486.379.600
└─└─└─

Complement C3-C5 Convertases

Complement C3-C5 Convertases D050577 - D12.776.124.486.274.045.387
└─└─└─

Facteur D du complément

Complement Factor D D011416 - D12.776.124.486.274.045.450
└─└─└─

Complément C1q

Complement C1q D015922 - D12.776.124.486.274.050.270
└─└─└─

Complément C1r

Complement C1r D015923 - D12.776.124.486.274.050.280
└─└─└─

Complément C1s

Complement C1s D003173 - D12.776.124.486.274.050.290
└─└─└─

Complément C2a

Complement C2a D050678 - D12.776.124.486.274.150.500
└─└─└─

Complément C2b

Complement C2b D050679 - D12.776.124.486.274.150.750
└─└─└─

Complément C3a

Complement C3a D015926 - D12.776.124.486.274.250.250
└─└─└─

Complément C3b

Complement C3b D003179 - D12.776.124.486.274.250.260
└─└─└─

Complément C4a

Complement C4a D015934 - D12.776.124.486.274.350.250
└─└─└─

Complément C4b

Complement C4b D015935 - D12.776.124.486.274.350.260
└─└─└─

Complément C5a

Complement C5a D015936 - D12.776.124.486.274.450.250
└─└─└─

Complément C5b

Complement C5b D050776 - D12.776.124.486.274.450.625
└─└─└─

Protéines inhibitrices de la fraction C3b du complément

Complement C3b Inactivator Proteins D003180 - D12.776.124.486.274.920.325
└─└─└─

Protéine de liaison à C4b

Complement C4b-Binding Protein D050716 - D12.776.124.486.274.920.662
└─└─└─└─

Alternative pathway C3-C5 Convertases

Complement C3-C5 Convertases, Alternative Pathway D050578 - D12.776.124.486.274.045.387.500
└─└─└─└─

Classical pathway C3-C5 Convertases

Complement C3-C5 Convertases, Classical Pathway D050579 - D12.776.124.486.274.045.387.750
└─└─└─└─

Mannose-Binding Protein-Associated Serine Proteases

Mannose-Binding Protein-Associated Serine Proteases D050606 - D12.776.124.486.274.045.387.875
└─└─└─└─

Complément C3c

Complement C3c D015932 - D12.776.124.486.274.250.260.500
└─└─└─└─

Complément C3d

Complement C3d D015933 - D12.776.124.486.274.250.260.750
└─└─└─└─

Complément C5a des-Arg

Complement C5a, des-Arginine D015937 - D12.776.124.486.274.450.250.255
└─└─└─└─

Facteur I du complément

Complement Factor I D017244 - D12.776.124.486.274.920.325.210
└─└─└─└─└─

Alternative pathway complement C3 convertase

Complement C3 Convertase, Alternative Pathway D051561 - D12.776.124.486.274.045.387.500.374
└─└─└─└─└─

Alternative pathway C5 convertase

Complement C5 Convertase, Alternative Pathway D051566 - D12.776.124.486.274.045.387.500.750
└─└─└─└─└─

Classical pathway complement C3 convertase

Complement C3 Convertase, Classical Pathway D051574 - D12.776.124.486.274.045.387.750.500
└─└─└─└─└─

Classical pathway C5 convertase

Complement C5 Convertase, Classical Pathway D051577 - D12.776.124.486.274.045.387.750.750

Auteurs principaux

H E Hinson

1 publication dans cette catégorie

Affiliations :
  • Departments of Neurology (Drs Hinson and Agarwal and Mr Myers) and Radiology (Drs Li and Pollock), and Division of Bioinformatics & Computational Biology, Department of Medical Informatics and Clinical Epidemiology (Dr McWeeney), Oregon Health & Sciences University, Portland.

Peter Li

1 publication dans cette catégorie

Loren Myers

1 publication dans cette catégorie

Chinar Agarwal

1 publication dans cette catégorie

Jeffrey Pollock

1 publication dans cette catégorie

Shannon McWeeney

1 publication dans cette catégorie

Jonas Mattisson

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Marcus Danielsson

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Maria Hammond

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Hanna Davies

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Caroline J Gallant

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Jessica Nordlund

1 publication dans cette catégorie

Affiliations :
  • Department of Medical Sciences, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Amanda Raine

1 publication dans cette catégorie

Affiliations :
  • Department of Medical Sciences, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Malin Edén

1 publication dans cette catégorie

Affiliations :
  • Department of Public Health and Caring Sciences / Geriatrics, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Lena Kilander

1 publication dans cette catégorie

Affiliations :
  • Department of Public Health and Caring Sciences / Geriatrics, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Martin Ingelsson

1 publication dans cette catégorie

Affiliations :
  • Department of Public Health and Caring Sciences / Geriatrics, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Jan P Dumanski

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
  • Faculty of Pharmacy, 3P Medicine Laboratory, International Research Agendas Programme, Medical University of Gdańsk, Gdańsk, Poland.
Publications dans "Immunoprotéines" :

Jonatan Halvardson

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Publications dans "Immunoprotéines" :

Lars A Forsberg

1 publication dans cette catégorie

Affiliations :
  • Department of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden. lars.forsberg@igp.uu.se.
  • The Beijer Laboratory, Uppsala University, Uppsala, Sweden. lars.forsberg@igp.uu.se.
Publications dans "Immunoprotéines" :

Lijun You

1 publication dans cette catégorie

Affiliations :
  • College of Biological Science and Engineering, Fuzhou University, Fuzhou 350116, China. Electronic address: ibptylj@fzu.edu.cn.
Publications dans "Immunoprotéines" :

Sources (11 au total)

Incorporating Immunoproteins in the Development of Classification Models of Progression of Intracranial Hemorrhage After Traumatic Brain Injury.

To define clinical, radiographic, and blood-based biomarker features to be incorporated into a classification model of progression of intracranial hemorrhage (PICH), and to provide a pilot assessment ... Patients with hemorrhage on admission head computed tomography were identified from a prospectively enrolled cohort of subjects with traumatic brain injury. Initial and follow-up images were interpret... We identified 106 patients, 36% had PICH. Dichotomized admission Glasgow Coma Scale (P = .004), Marshall score (P = .004), and 3 PCs were significantly associated with PICH. For the CV only model, sen... In this pilot investigation, we observed that composites of IPs may improve PICH classification models when combined with CVs. However, overall model performance must be further optimized; results wil...

Model establishment of prognostic-related immune genes in laryngeal squamous cell carcinoma.

Laryngeal squamous cell carcinoma (LSCC) is one of the most common malignant tumors of the head and neck in the world. At present, the treatment methods include surgery, radiotherapy, and chemotherapy... We collected the 111 cases of laryngeal squamous cell carcinoma and 12 matched normal samples in the The Cancer Genome Atlas Database (TCGA) gene expression quantification database. The differentially... We selected 8 immune-related genes that can predict the prognosis of LSCC in a COX regression model and plotted the Kaplan-Meier survival curve. The 5-year survival rate of the high-risk group was 16.... We screened out 8 immune genes related to prognosis: RBP1, TLR2, AQP9, BTC, EPO, STC2, ZAP70, and PLCG1 to construct risk value models, which can be used to speculate the prognosis of the disease and ...

The vaginal immunoproteome for the prediction of spontaneous preterm birth: A retrospective longitudinal study.

Preterm birth is the leading cause of neonatal morbidity and mortality worldwide. Most cases of preterm birth occur spontaneously and result from preterm labor with intact (spontaneous preterm labor [... Vaginal swabs were collected across gestation from pregnant women who ultimately underwent term birth, sPTL, or PPROM. Cytokines, chemokines, growth factors, and antimicrobial peptides in the samples ... Throughout uncomplicated gestation, the vaginal immunoproteome harbors a cytokine network with a homeostatic profile. Yet, the vaginal immunoproteome is skewed toward a pro-inflammatory state in pregn... The vaginal immunoproteome undergoes homeostatic changes throughout gestation and deviations from this shift are associated with sPTB. Furthermore, the vaginal immunoproteome can be leveraged as a pot... This research was conducted by the Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research,...

Conformation-selective rather than avidity-based binding to tumor associated antigen derived peptide-MHC enables targeting of WT1-pMHC low expressing cancer cells by anti-WT1-pMHC/CD3 T cell engagers.

T cell engagers, a category of T cell-retargeting immunotherapy, are rapidly transforming clinical cancer care. However, the lack of tumor-specific targets poses a significant roadblock for broad adap...

KIR3DL3-HHLA2 and TMIGD2-HHLA2 pathways: The dual role of HHLA2 in immune responses and its potential therapeutic approach for cancer immunotherapy.

T cells and natural killer (NK) cells are essential components of the immune system and are regulated by coinhibitory and costimulatory molecules in which the B7 family and CD28 family play significan... Here, we reviewed recent studies about HHLA2 ligand interactions with KIR3DL3 and TMIGD2. We focused on elucidating the pathways between KIR3DL3/TMIGD2 and HHLA2 as well as their function in tumour pr... KIR3DL3/TMIGD2-HHLA2 may represent novel pathways within the tumour microenvironment and serve as crucial immune checkpoints for developing novel therapeutic drugs against human cancer....

Exploration of Immune-Related Gene Expression in Osteosarcoma and Association With Outcomes.

Host immune dysregulation is associated with initiation and development of osteosarcoma. In addition, immunotherapy for osteosarcomas requires some knowledge of the immune state of patients.... To perform an immunogenomic landscape analysis based on The Cancer Genome Atlas (TCGA) project, which provides osteosarcoma samples with clinical information.... This genetic association study was conducted from July 20, 2020, to September 20, 2020, as a secondary analysis of public data. Cox regression and risk score analyses were used to construct signatures... Differentially expressed genes (DEGs) were analyzed between groups, and potential molecular mechanisms, expression regulation, and immune cell infiltration were also explored using bioinformation meth... In this genetic association study based on 84 samples from patients with osteosarcoma from TCGA (mean [SD] age, 15.0 [4.8] years; 47 [56.0%] men; mean [SD] follow-up time, 4.1 [2.8] years), a total of... This genetic association study developed a prognostic modeling tool for osteosarcoma based on IRG expression profiles, which could result in improved survival rates through more individualized therapi...