Application of anti-PD-1 antibody and/or anti-PD-L1 antibody in preparation of medicine for treating Parkinson's disease
A PD-L1, PD-1 technology, applied in the field of medicine, can solve the problem of not using Parkinson's disease
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Embodiment 1
[0021] Example 1 The effect of anti-PD-1 / PD-L1 antibody on the α-polynucleoprotein oligomer of Parkinson mouse
[0022] In this example, the method of Luk et al. (Luk KC, Kehm V, Carroll J, Zhang B, O'Brien P, Trojanowski JQ, Lee V. Pathological α-Synuclein Transmission Initiates Parkinson-like Neurodegeneration in Nontransgenic Mice. Science. 2012 ; 338:949–953.) Induce Parkinson's rats. The procedure is as follows: 15 μg α-synuclein fibrils are injected into the striatum of male C57BL / 6 mice. After 60 days, the above-mentioned male C57BL / 6 mice were divided into groups, 10 mice in each group, and the drugs to be tested were injected intravenously: pembrolizumab, tislelizumab, nivolumab, cimiprizumab, carbo Relilizumab, teriprizumab, sintilizumab, as well as atelizumab, avenrizumab, and devaluzumab, each drug is injected in two doses, specific injections The dosage is shown in Table 1, and the injection is performed every 10 days. In addition, male C57BL / 6 mice injected with P...
Embodiment 2
[0036] Example 2 Preparation of oral emulsion
[0037] The preparation method of the emulsion includes the following steps: the anti-PD-1 antibody and / or the anti-PD-L1 antibody are dissolved in a PBS buffer containing 4% Tween-80 at a ratio of 50 mg: 1 mL as an aqueous phase, as follows: 500mg pembrolizumab was dissolved in 10mL PBS buffer containing 4% Tween-80 as the water phase; olive oil containing 6% lecithin was used as the oil phase; then the water phase and the oil were mixed in equal volumes at 3000 revolutions After shaking for 2 minutes, stir at 30000 rpm for 5 minutes.
Embodiment 3
[0038] Example 3 Clinical experiment
[0039] Clinical evaluation uses the Parkinson’s Disease Comprehensive Assessment Scale (MDS-UPDRS) (refer to https: / / www.movementdisorders.org / MDS / MDS-Rating-Scales / MDS-Unified-Parkinsons-Disease-Rating-Scale-MDS-MDS -MDS-UPDRS.htm). The experiment lasted for 12 months. Patients with Parkinson's disease should be diagnosed by a professional doctor as the inclusion criteria. Patients who were tolerant to levodopa drugs were excluded from this experiment. In this example, before the experiment, the patient appropriately reduced the dose of the Parkinson's disease treatment drug levodopa-like drugs used in the early stage, so that the symptoms were obvious. The anti-PD-1 / PD-L1 antibody drug used in this example is a commercial clinical drug, and the usage and dosage of intravenous injection refer to its usage and dosage in anti-cancer treatment.
[0040] Case 1:
[0041] Female, age: 78, weight: 65 kg, height: 1.60 meters, was diagnosed with P...
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