Drug Database
RA

rabies antiserum

✓ Approved

Shanghai Serum Biotechnology · Polyclonal Antibodies · Polyclonal Antibodies

What is rabies antiserum?

rabies antiserum is a polyclonal antibodies developed by Shanghai Serum Biotechnology. It is approved for therapeutic indications via injectable (others) or intramuscular (im) injection.

Drug Profile

CompanyShanghai Serum Biotechnology
Drug ClassPolyclonal Antibodies, Antibody
RouteInjectable (Others), Intramuscular (IM) Injection
StatusApproved

Therapeutic Indications

rabies antiserum is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Infections and infestationsRabies✓ Approved

Related Research Articles

PubMedFrontiers in immunology2026-09-19

Biological barriers underlying the extremely high fatality of symptomatic rabies: neuroinvasion, immune evasion, and blood-brain barrier restriction.

Sun Chen C, Guo Xiao X, Xiao Liang L, Wang Wenxin W et al.

Rabies remains one of the most preventable fatal infections, yet once clinical symptoms appear, survival is exceedingly rare. This paradox cannot be explained simply by the absence of a single effective antiviral drug. In this review, we frame symptomatic rabies as a sequential barrier-driven disease process in which neuroinvasion, immune evasion, and blood-brain barrier restriction converge to make post-symptom rescue biologically difficult. Rabies virus first changes the anatomical battlefield by entering peripheral nerves, exploiting receptor-supported uptake and retrograde axonal transport, and establishing infection within protected neural circuits. It then delays the host counterattack through weak or strain-dependent innate sensing, viral interference with interferon and signal transducer and activator of transcription (STAT) signaling, and insufficient conversion of peripheral immune activation into effective central nervous system clearance. Once central nervous system (CNS) infection is established, blood-brain barrier restriction further limits access of neutralizing antibodies, antiviral compounds, biologics, and immune cells to infected neural tissue. The convergence of these barriers permits CNS persistence and drives fatal encephalopathy, characterized less by widespread neuronal destruction than by synaptic, dendritic, circuit, autonomic, and functional collapse. Recent experimental advances, including CNS-accessible antibody strategies, blood-brain barrier (BBB)-modulating approaches, monoclonal antibody therapy, and One Medicine models, suggest that symptomatic rabies may require stage-specific therapeutic combinations rather than a single rescue intervention. We propose that future rabies therapy should be organized around three translational windows: preventing neuroinvasion before CNS entry, achieving immune-assisted viral control during early CNS infection, and combining CNS viral clearance with neuroprotective and autonomic support once encephalopathy is established. However, most mechanistic and therapeutic evidence remains derived from cellular and animal models, and clinical validation of CNS-directed or barrier-targeted interventions in symptomatic human rabies remains limited. Breaking the barrier cascade may be the central requirement for making symptomatic rabies treatable.

PubMedBrain research bulletin2026-09-19

Rabies and distemper exhibit distinct patterns of axonal damage and apoptotic cell death in the central nervous system of dogs and foxes.

Pfetzing Sarah S, Freuling Conrad C, Puff Christina C, Kammeyer Patricia P et al.

Rabies is a fatal zoonosis caused by the rabies virus (RABV), which enters the central nervous system via a retrograde axonal pathway with histopathologically often very subtle but fatal polioencephalitis. Distemper is characterized by neuronal and/or axonal damage, as well as leukoencephalitis with demyelination in dogs and polioencephalitis without demyelination in foxes. This study aimed to compare the neuropathological lesions and the amount of axonal damage and apoptosis in the central nervous system of dogs and foxes infected with RABV or canine distemper virus (CDV), alongside non-infected control groups. Staining with hematoxylin and eosin, luxol fast blue-nuclear fast red, and immunohistochemistry for lyssaviral nucleoprotein, CDV nucleoprotein, β-amyloid precursor protein (a marker for early axonal damage) and active caspase-3 (a marker for apoptosis) was performed on archival formaldehyde-fixed, paraffin-embedded brain specimens. Dogs and foxes infected with RABV showed no change in the number of active caspase-3-immunoreactive cells and β-amyloid precursor protein-immunoreactive axons and no demyelinating areas. In contrast, CDV infection was characterized by an increase in active caspase-3-immunoreactive cells and β-amyloid precursor protein-immunoreactive axons in both species, and additionally demyelinating areas in the dog. These results suggest that RABV effectively evades recognition by intrinsic neuroaxonal antiviral mechanisms on its route to the central nervous system.

PubMedJournal of molecular neuroscience : MN2026-09-19

ABCC9/SUR2 has a Complex Expression Pattern in Human Brain Gliovascular Unit Cells, Including Astrocytes.

Katsumata Yuriko Y, Morganti Josh M JM, Liao Andrew A, Zhou Wei W et al.

The ABCC9 gene and its cognate protein SUR2 play important roles in neurovascular coupling and are implicated in hippocampal sclerosis of aging (HS-Aging). However, prior studies have not focused on human brain SUR2 expression or SUR2 in glial cells. Here we analyzed cell type-specific ABCC9/SUR2 expression patterns, and correlation with known genetic risk variants, using multiple data sets and a novel antiserum. Existing single-nucleus RNA sequencing data sets and new spatial transcriptomics data indicated that SUR2 transcripts were expressed primarily in human brain pericytes, astrocytes, smooth muscle cells, and endothelial cells. Evaluation of Sur2 expression in a sample of mice brains showed similar results except Sur2 was not detected in the mice astrocytes. In a SUR2-enriched subcluster of human astrocytes, the pattern of transcript expression suggested responsiveness to thyroid hormone signaling: SUR2-correlated gene products were enriched for thyroid hormone-sensitive transcripts and SLCO1C1, the astrocyte thyroid hormone importer, was the transcript with the strongest correlation with SUR2 expression. Cells in the SUR2 + astrocyte cluster tended to have been derived from individuals lacking severe Alzheimer's disease pathology. An ABCC9 single nucleotide variant (rs1914361, also a HS-Aging risk allele) was associated with increased SUR2 expression in astrocytes, but not other cell types. SUR2 mRNA splicing differed between cell types; astrocytes preferentially expressed the SUR2B variant. A novel SUR2 antiserum immunolabeled blood vessel walls and some astrocyte-morphology cells in human brain. Overall, human brain SUR2 expression was enriched among different cell types of the gliovascular unit. A SUR2-enriched, possibly-homeostatic astrocyte subcluster suggested connections to thyroid hormone signaling.

PubMedCell reports2026-09-18

Antigenic landscape of rabies and related lyssaviruses revealed by cryo-EM.

Callaway Heather M HM, Zyla Dawid S DS, Hastie Kathryn M KM, Harkins Stephanie S SS et al.

Rabies continues to kill over 60,000 people per year despite life-saving vaccines and post-exposure treatments and costs billions of dollars in prevention and treatment. Preventing rabies deaths and reducing the global economic burden of the virus will require both developing a monoclonal antibody cocktail to replace human serum in treatment and improving rabies vaccines to elicit long-lasting protection. Here, we solve nine cryo-electron microscopy (cryo-EM) structures of neutralizing monoclonal antibodies (mAbs) in complex with the rabies virus glycoprotein (RABV-G). The nine structures span three known antigenic sites plus two additional antigenic sites, not among the five classically identified sites. We find that these antigenic sites, V and VI, are broadly cross-reactive across lyssaviruses, whereas immunodominant sites II/IV and III are rabies specific. Across the mAb panel, fusion inhibition and binding affinity correlate best with neutralization. Together, these results provide a roadmap for structure-guided vaccine and therapeutic antibody design for rabies and related lyssaviruses.

PubMedFrontiers in public health2026-09-18

From one-size-fits-all to context-specific: the 10-day observation rule-a need for change.

Wang Xin X

WHO's 'Zero by 30' strategic plan relies on post-exposure prophylaxis guidelines designed for high-resource settings. This policy brief argues that the implementation gap of the 10-day observation rule in high-burden countries stems from fundamental infeasibility, exposing two paradigm defects in WHO guideline development: one-size-fits-all thinking and insufficient attention to implementation science. When the public misinterprets the 10-day rule as "wait and see" rather than "initiate PEP immediately while observing the animal," three biological facts render this misinterpretation fatal: symptomatic rabies is nearly 100% fatal and untreatable; a single vaccine dose cannot promptly induce sufficient neutralizing antibodies; and the incubation period for craniofacial Category III bites can be as short as 5-10 days-shorter than the full observation window. Waiting for animal observation without initiating PEP during this window means missing the only opportunity for effective prevention. Evidence from multiple countries shows that the rule's preconditions are almost never met in settings where 95% of rabies deaths occur. This misinterpretation has led to preventable deaths and given rise to guideline-associated rabies phobia (GARP). We propose five revisions to refine-not discard-the rule. Reshaping the paradigm is an ethical prerequisite for achieving 'Zero by 30'.

PubMedeLife2026-09-18

An applicable and efficient retrograde monosynaptic circuit mapping tool for larval zebrafish.

Chen Tian-Lun TL, Deng Qiu-Sui QS, Lin Kunzhang K, Zheng Xiu-Dan XD et al.

The larval zebrafish is a vertebrate model for in vivo monitoring and manipulation of whole-brain neuronal activity. Tracing its neural circuits remains challenging. Here, we report an applicable methodology tailored for larval zebrafish to achieve efficient retrograde trans-monosynaptic tracing from genetically defined neurons via EnvA-pseudotyped glycoprotein-deleted rabies viruses. By combinatorially optimizing multiple factors involved, we identified the CVS strain trans-complemented with advanced expression of N2cG at 36 °C as the optimal combination. It yielded a tracing efficiency of up to 20 inputs per starter cell. Its low cytotoxicity enabled the viable labeling and calcium imaging of infected neurons 10 days post-infection, spanning larval ages commonly used for functional examination. Cre-dependent labeling was further developed to enable cell-type-specific input tracing and circuit reconstruction. We mapped cerebellar circuits and uncovered the ipsilateral preference and subtype specificity of granule cell-to-Purkinje cell connections. Our method offers an efficient way for tracing neural circuits in larval zebrafish.

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