大规模的“二阳”要来了？专家最新研判来了！
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; font-size: 16px; letter-spacing: 1px;">“二阳”等相关话题</span>
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; font-size: 16px; letter-spacing: 1px;">引发网友热议</span>
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; font-size: 16px; letter-spacing: 1px;">↓↓↓</span>
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px;font-family: Helvetica, Arial, sans-serif;">5月15日下午，在来瑞特韦上市后临床研究启动仪式上，共和国勋章获得者、中国工程院院士钟</span><span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px; box-sizing: border-box !important; overflow-wrap: break-word !important; line-height: 1.56em;font-family: Helvetica, Arial, sans-serif;">南山说，目前在广州流行的主流新冠病毒株是XBB1.9.1。</span><span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px;font-family: Helvetica, Arial, sans-serif;">根据目前广州市发热门诊的数据，在接受检测的发热病人里，有20%-25%是新冠病毒感染者。</span>
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px;font-family: Helvetica, Arial, sans-serif;"><span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px;font-family: Helvetica, Arial, sans-serif;">钟南山介绍，无论有症状还是没有症状，如果体内新冠病毒对应的抗体增 高，就说明人体曾被感染过。从这个角度看，根据测定，</span><span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px; color: #007aaa;font-family: Helvetica, Arial, sans-serif;"><strong style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; box-sizing: border-box !important; overflow-wrap: break-word !important;">全国大概有85%的人感染过新冠病毒，约有11亿至12亿人。</strong></span></span>
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<span style="color: #222222; font-size: 16px; letter-spacing: 1px; white-space: pre-wrap; caret-color: rgba(0, 0, 0, 0.9);font-family: Helvetica, Arial, sans-serif;">钟南山说，根据相关实验室研究和新加坡等地的真实世界研究，新冠病毒感染后产生的抗体能在4-6个月的时间内起到保护人体的作用；但如果面对变异株XBB，其保护力可能会减弱，“从去年12月算起，实际看现在已经是到了这个时间了。”</span>
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px; box-sizing: border-box !important; overflow-wrap: break-word !important; line-height: 1.56em;font-family: Helvetica, Arial, sans-serif;">钟南山透露，下一步应对新冠病毒感染，一方面还需要研发能覆盖XBB变异毒株的疫苗，包括MRNA疫苗和重 组蛋白疫苗，这些疫苗主要是针对一些特殊人群，比如免疫低下或有其他严重基础病的老年人；另一方面，一旦感染了新冠，应及时给予药物治疗，能大大降低死亡率。</span>
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<span style="margin: 0px; padding: 0px; outline: 0px; max-width: 100%; color: #222222; text-align: justify; white-space: pre-wrap; text-decoration-thickness: initial; font-size: 16px; letter-spacing: 1px; box-sizing: border-box !important; overflow-wrap: break-word !important; line-height: 1.56em;font-family: Helvetica, Arial, sans-serif;">据了解，来瑞特韦是我国首款单药3CL抗新冠1类创新药，已在3月获批附条件上市，用于治疗新冠轻中症成年患者，研究表明该药的抗病毒效果与辉瑞Paxlovid效果相当，且有效避免了因联用利托那韦产生的毒副作用。</span>
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