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anti-D immunoglobulin

✓ Approved

Kedrion · 多克隆抗体 · 多克隆抗体

什么是 anti-D immunoglobulin?

anti-D immunoglobulin 是一种多克隆抗体,由Kedrion研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intramuscular (IM) Injection。

药物档案

公司Kedrion
药物类别多克隆抗体, 细胞治疗, 抗体
给药途径Injectable (Others), Intramuscular (IM) Injection
状态Approved

治疗适应症

anti-D immunoglobulin 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Congenital, familial and genetic disordersRhesus haemolytic disease of newborn✓ Approved

相关研究文献

PubMedFrontiers in immunology2026-08-04

Case Report: Overlapping multiple sclerosis and neuropsychiatric systemic lupus erythematosus with positive MOG-IgG: a case initially misdiagnosed as depression.

Wei Wan W, Jin Tao T, Zhang Liuhai L, Sun Yumeng Y et al.

We present a 69-year-old female patient who initially manifested with depression and anhedonia, initially misdiagnosed as primary psychiatric illness. She subsequently developed progressive gait instability and cognitive decline. After comprehensive clinical and laboratory evaluation, she was finally diagnosed with multiple sclerosis (MS) complicated by neuropsychiatric systemic lupus erythematosus (NPSLE). Brain magnetic resonance imaging (MRI) revealed multifocal white matter lesions consistent with demyelination. Serologic testing demonstrated positivity for antinuclear antibody (ANA), anti-double-stranded DNA (dsDNA), anti-SS-A/Ro, anti-histone, anti-nucleosome, and anti-centromere antibodies. Cerebrospinal fluid (CSF) examination confirmed intrathecal synthesis of immunoglobulin G (IgG), as evidenced by CSF-restricted oligoclonal bands (OCBs). Serum myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG) was positive at a titer of 1:32, whereas aquaporin-4 (AQP4) antibodies were negative. Based on the clinical manifestations, laboratory results and disease progression, the final diagnosis was established as coexisting MS and NPSLE. The patient achieved clinical improvement after treatment with glucocorticoids and hydroxychloroquine. This case highlights the diagnostic challenges posed by overlapping autoimmune central nervous system (CNS) disorders and underscores the importance of longitudinal assessment in differentiating MS from MOG-IgG-associated disorder (MOGAD) and NPSLE.

PMID 42548805
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PubMedCell2026-08-04

Co-option of retrotransposons promotes antibody diversification.

Lauring Max C MC, Yang Ming M, Sarode Aditya A, Wang Jianhua J et al.

Activation-induced cytidine deaminase (AID) accomplishes somatic hypermutation (SHM) of VH(D)JH genes in germinal center B cells for antibody diversification and affinity maturation. How AID specifically targets VH(D)JH remains unclear. We report the discovery of LINE-1 (L1) retrotransposons upstream to many VH genes in the immunoglobulin locus. These L1s are evolutionarily old, truncated, and retrotransposition dead. Recombined VH promoters generate long, strong antisense RNAs encoding upstream L1s, triggering the human silencing hub (HUSH) complex and AID recruitment, which we term L1-driven SHM. We show that L1-driven SHM occurs in vivo using HUSH conditional knockout mice and engineered mice with VH genes devoid of upstream L1s. Insertion of transcriptionally active L1s at non-immunoglobulin loci endogenously lacking upstream L1s promotes off-target SHM. We demonstrate that old retrotransposons serve physiological roles, and our findings reveal how B cells co-opted an anti-retrotransposon silencing mechanism to promote antibody diversity. In doing so, we established a new link between cell-intrinsic innate and adaptive immunity.

PMID 42546688
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PubMedFujita medical journal2026-08-04

A case of anti-N-methyl-D-aspartate receptor antibody encephalitis associated with immature ovarian teratoma.

Ohwaki Akiko A, Isomura Kurumi K, Takada Kyohei K, Ito Mayuko M et al.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is typically associated with mature cystic teratomas. We report a case of anti-NMDA receptor encephalitis associated with an immature ovarian teratoma, which is a malignant tumor. A 16-year-old girl who presented with impaired consciousness and abnormal behavior was referred to our hospital. After evaluation upon admission, she was diagnosed with anti-NMDA receptor encephalitis associated with an ovarian mature cystic teratoma, and laparoscopic right salpingo-oophorectomy was performed. The postoperative pathological diagnosis confirmed the presence of an immature ovarian teratoma. The patient subsequently underwent immunoglobulin therapy, steroid pulse therapy, and plasma exchange for the treatment of encephalitis. Bleomycin, etoposide, and cisplatin chemotherapy was administered after her symptoms improved. In this case, early collaboration among the departments of neurology, obstetrics and gynecology, and emergency medicine enabled a prompt diagnosis and effective treatment. The patient's symptoms were successfully ameliorated through early removal of the tumor and pharmacotherapy. Although anti-NMDA receptor encephalitis generally has a favorable prognosis, early diagnosis and initiation of treatment considerably affect the outcome. Clinicians should suspect anti-NMDA receptor encephalitis when a young patient presents with impaired consciousness or abnormal behavior and consider the possibility of underlying malignant tumors.

PMID 42549471
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PubMedSmall (Weinheim an der Bergstrasse, Germany)2026-08-04

Smart, Gravity-Driven, Dual-Mode, Disposable Evanescent Wave Fluorescent Optofluidic Bio-Nanochip for Rapid and Sensitive Point-of-Need Testing of Trace Pollutants.

Liu Siyan S, Liu Jiayuan J, Ye Yiqiang Y, Zhao Yikan Y et al.

The decentralization of biosensing to point-of-need (PON) settings necessitates single-use devices that combine laboratory-level sensitivity with field-deployable simplicity. Existing fluorescent optofluidic chips achieve high sensitivity but rely on bench-top optics, pumps, and trained personnel. Here, we present a smart, disposable evanescent wave fluorescent optofluidic bio-nanochip (DEFOB) that bridges this performance gap. The DEFOB integrates a gravity-driven, 3D-printed microfluidic chip with a functionalized tapered fiber nanosensor, a compact alignment-free all-fiber optical reader, and a smartphone application. This synergistic design enables ultrasensitive, quantitative detection in both homogeneous and heterogeneous assay formats without the need for external pumps or complex peripherals. We demonstrate the platform's versatility through the laboratory-comparable quantification of sulfamerazine antibiotics via immunoassay and of SARS-CoV-2 via an integrated RAA-CRISPR/Cas12b assay, achieving detection limits of 0.06 µg/L and 0.70 copies/µL, respectively. By combining dual-mode operation, high sensitivity, quantitative accuracy, intelligence, plug-and-play functionality, and a low-cost workflow, the DEFOB platform represents a paradigm shift in PON testing, with broad applications in clinical diagnostics, environmental monitoring, and global health security.

PMID 42549630
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PubMedPain medicine case reports2026-08-04

Ultrasound-Guided Stellate Ganglion and Interscalene Blocks for Refractory Pediatric Parsonage-Turner Syndrome: A Case Report and Clinical Implications.

Laraib Warda W, Abbas Adeel A, Habib Insha I, Fareh Zohad Z et al.

Parsonage-Turner syndrome (PTS) is an uncommon inflammatory brachial plexopathy; pediatric and bilateral cases are rare, and evidence for managing refractory pediatric pain is limited. A previously healthy 6-year-old girl developed sudden severe left upper-limb pain with progressive wrist-drop in August 2023; by October, the right arm was affected. Nerve conduction studies/electromyography confirmed brachial plexopathy and magnetic resonance imaging showed diffuse thickening of left C5-C7. Laboratory tests were unremarkable, except for an isolated anti-glycosphingolipid monosialo-2 antibody. Oral corticosteroids, tramadol, and 2 intravenous immunoglobulin doses produced limited benefit, and corticosteroids caused mood disturbance. In October 2023, ultrasound-guided stellate ganglion (C6) and interscalene (C5-C6) blocks with 4-6 mL of 0.25% bupivacaine under general anesthesia were performed. At one week, she reported ~85% pain relief; analgesics were reduced to paracetamol. In refractory pediatric bilateral PTS, regional stellate ganglion and interscalene blocks provided rapid, substantial analgesia; prospective studies should define indications and long-term outcomes.

PMID 42550561
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PubMedMolecular biology reports2026-08-04

Diagnostic and therapeutic significance of selected antibodies against advanced glycation end-products (anti-AGEs).

Sobczyńska Julia J, Federowicz Jakub J, Galińska Zuzanna Z, Ziomek Maciej M et al.

The aim of this review is to summarize current knowledge on the diagnostic and therapeutic significance of antibodies against advanced glycation end-products (anti-AGEs). AGEs are formed through non-enzymatic reactions of reducing sugars with proteins, lipids, and nucleic acids, and their accumulation has been implicated in the pathogenesis of chronic diseases such as diabetes, atherosclerosis, cancer, and neurodegenerative disorders. This paper discusses anti-MGO modified proteins, anti-imidazolone, anti-pentosidine, anti-CML (including SIWA318H), anti-CEL, anti-CMA, and anti-GA-pyridine antibodies, with a focus on their potential applications in diagnostics (biomarkers, disease progression monitoring) and therapy (e.g., SIWA318H in pancreatic cancer). The review also highlights current limitations, particularly regarding clinical use in humans, and outlines perspectives for further research in this promising field.

PMID 42550329
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