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Poliomyelitis

Poliomyelitis

Poliomyelitis is an infectious disease caused by a virus that may lead to paralysis by damaging the nervous system. At Protheragen, we are deeply committed to unique research in treatment methodologies and modeling pertaining to poliomyelitis. We intend to provide end-to-end therapeutic development solutions to commercialization for poliomyelitis.

Overview of Poliomyelitis

Poliomyelitis (polio) is an infectious disease caused by the poliovirus which belongs to the Picornaviridae family and genus Enterovirus. Polio primarily infects motor neurons in the anterior horn of the spinal cord and brainstem , leading to flaccid paralysis. The disease occurs in four forms:

Clinical Form Frequency Key Features
Asymptomatic Infection ~72% of cases No noticeable symptoms; immune system clears virus without clinical signs.
Abortive Poliomyelitis ~24% of cases Mild, non-specific symptoms (fever, headache, sore throat, vomiting).
Non-Paralytic Poliomyelitis ~4% of cases Aseptic meningitis (neck stiffness, photophobia); no motor deficits.
Paralytic Poliomyelitis <1% of cases Flaccid paralysis (acute onset, asymmetrical).

Pathogenesis of Poliomyelitis

Poliomyelitis occurs when the poliovirus infects the central nervous system following replication in the oropharynx and intestines due to neural tropism via CD155 receptors on motor neurons. The virus disseminates either through blood or retrograde axonal transport, selectively infecting and destroying anterior horn cells in the spinal cord and brainstem motor nuclei. This leads to inflammatory infiltrates, neuronophagia, and subsequent flaccid paralysis from motor neuron loss.

Pathological mechanism of poliomyelitis.Fig.1 Schematic diagram of the pathological mechanism of poliomyelitis. (Mbani C J, et al., 2023)

Therapeutic Development for Poliomyelitis

Drug Names Mechanism of Action Targets NCT Number Research Phase
nOPV1+nOPV2 Genetically stabilized live-attenuated vaccines inducing mucosal IgA and systemic IgG responses against poliovirus types 1 & 2 Poliovirus capsid proteins, CD155 receptor on host cells NCT06895486 Phase II
nOPV3 Same as above, targeting poliovirus type 3 with enhanced genetic stability to prevent reversion Poliovirus type 3 capsid proteins, CD155 receptor NCT05654467 Phase II

Disclaimer: Protheragen focuses on providing preclinical research services. This table is for information exchange purposes only. This table is not a treatment plan recommendation. For guidance on treatment options, please visit a regular hospital.

Our Services

As a provider of preclinical research services for poliomyelitis, Protheragen offers comprehensive solutions in diagnostic and therapeutic development. We have expertise in developing physiologically relevant models for in depth biomarker discovery and validation as well as optimization of therapeutic efficacy which include in vitro models, animal models and specialized blood-brain barrier (BBB) models tailored for the central nervous system (CNS).

Therapeutic Development Services

Disease Model Development Services

Animal Model Development

PVR Transgenic Mouse Model: These mice are engineered to express the human poliovirus receptor (hPVR), making them susceptible to poliovirus infection, unlike normal mice. The mice can be infected via intravenous or intramuscular injection, as well as through direct inoculation into the spinal cord or brain.

Protheragen is steadfastly dedicated to meticulously validating and optimizing therapies for poliomyelitis through a thorough series of pharmacodynamics (PD), pharmacokinetics (PK) and toxicology studies. If you are interested in our services, please feel free to contact us for more details and quotation information of related services.

Reference

  • Mbani C J, Nekoua M P, Moukassa D, et al. The fight against poliovirus is not over[J]. Microorganisms, 2023, 11(5): 1323.
For research use only. Not intended for any clinical use.

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