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 加分100%浜中特選昆布鍋物有提供尾牙方案嗎？ 》公益路絕對要吃的10家餐廳｜台中人私藏推薦 |
| 知識學習｜其他 2025/11/21 05:54:24 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
身為一個熱愛美食、喜歡在城市裡挖掘驚喜的人，臺中公益路一直是我最常出沒的地方之一。這條路可說是「臺中人的美食戰場」，從精緻西餐到創意火鍋，從日式丼飯到義式早午餐，每走幾步，就會有完全不同的特色料理餐廳。 這次我特別花了一整個月，實際造訪了公益路上十間口碑不錯的餐廳。有的是網友熱推的打卡名店，也有隱藏在巷弄裡的小驚喜。我以環境氛圍、口味表現、價格CP值與再訪意願為基準，整理出這篇實測評比。希望能幫正在猶豫去哪裡吃飯的你，找到那一間「吃完會想再來」的餐廳。 評比標準與整理方向
這次我走訪的10家餐廳橫跨不同料理類型，從高質感牛排館到巷弄系早午餐，每一間都有自己獨特的風格。為了讓整體比較更客觀，我依照以下四大面向進行評比，並搭配實際用餐體驗來打分。
整體而言，我希望這份評比不只是「哪家好吃」，而是幫你在不同情境下（約會、家庭聚餐、朋友小聚、商業午餐）都能快速找到合適的選擇。畢竟，美食不只是味覺的滿足，更是一段段與朋友共享的生活記憶。 10間臺中公益路餐廳評比懶人包公益路向來是臺中人聚餐的首選地段，從火鍋、燒肉到中式料理與早午餐，每走幾步就有驚喜。以下是我實際造訪過的10間代表性餐廳清單，橫跨平價、創意、高級各路風格。
一頭牛日式燒肉｜炭香濃郁的和牛饗宴，約會聚餐首選
走在公益路上，很難不被 一頭牛日式燒肉 的木質外觀吸引。低調卻不失質感的門面，搭配昏黃燈光與暖色調的內裝，讓人一進門就感受到濃濃的日式職人氛圍。店內空間不大，但桌距規劃得宜，每桌皆設有獨立排煙設備，烤肉時完全不怕滿身油煙味。 餐點特色
一頭牛的靈魂，絕對是他們招牌的「三國和牛拼盤」。 用餐體驗整體節奏掌握得非常好。店員會在你剛想烤下一片肉時貼心遞上夾子、幫忙換烤網，讓人完全不用分心。整場用餐過程就像一場表演，從視覺、嗅覺到味覺都被滿足。 綜合評分
地址：408臺中市南屯區公益路二段162號電話：04-23206800 官網：http://www.marihuana.com.tw/yakiniku/index.html 小結語一頭牛日式燒肉不僅是「吃肉的地方」，更像是一場五感盛宴。從進門那一刻到最後一道甜點，都能感受到他們對細節的用心。 TANG Zhan 湯棧｜文青系火鍋代表，麻香湯底與視覺美感並重
在公益路這條美食戰線上，TANG Zhan 湯棧 是讓人一眼就會想走進去的那一種。 餐點特色
湯棧最有名的當然是它的「麻香鍋」。 用餐體驗整體氛圍比一般火鍋店更有質感。 綜合評分
地址：408臺中市南屯區公益路二段248號電話：04-22580617 官網：https://www.facebook.com/TangZhan.tw/ 小結語TANG Zhan 湯棧 把傳統火鍋做出新的樣貌保留臺式鍋物的溫度，又結合現代風格與細節服務，讓吃鍋這件事變得更有品味。 如果你想找一間兼具「好吃、好拍、好放鬆」的火鍋店，湯棧會是公益路上最有風格的選擇之一。 NINI 尼尼臺中店｜明亮寬敞的義式早午餐天堂
如果說前兩間是肉食愛好者的天堂，那 NINI 尼尼臺中店 絕對是想放鬆、聊聊天的好地方。餐廳外觀以白色系與大片玻璃窗為主，陽光灑進室內，讓人一踏入就有種度假般的輕盈感。假日早午餐時段特別熱鬧，建議提早訂位。 餐點特色
NINI 的菜單融合義式與臺灣人口味，選擇多樣且份量十足。主打的 松露燉飯 濃郁卻不膩口，米芯保留微Q口感；而 香蒜海鮮義大利麵 則以新鮮白蝦、花枝與淡菜搭配微辣蒜香，口感層次豐富。 用餐體驗店內氣氛輕鬆不拘謹，無論是一個人帶電腦工作、或朋友聚餐，都能找到舒服角落。餐點上桌速度穩定，服務人員態度親切、補水與收盤都非常主動。整體節奏讓人覺得「時間變慢了」，很適合想遠離忙碌日常的人。 綜合評分
地址：40861臺中市南屯區公益路二段18號電話：04-23288498 小結語NINI 尼尼臺中店是一間能讓人放下手機、慢慢吃飯的餐廳。餐點不追求浮誇，而是以「剛剛好」的份量與風味，陪伴每個平凡午後。如果你在找一間能邊吃邊聊天、拍照也漂亮的早午餐店，NINI 會是你在公益路上最不費力的幸福選擇。 加分100%浜中特選昆布鍋物｜平價卻用心的湯頭系火鍋，家庭聚餐好選擇
在公益路這條高質感餐廳林立的戰場上，加分100%浜中特選昆布鍋物 走的是截然不同的路線。它沒有浮誇的裝潢、也沒有高價位的套餐，但靠著實在的湯頭與親切的服務，默默吸引許多回頭客。每到用餐時間，總能看到家庭或情侶三兩成群地圍著鍋邊聊天。 餐點特色
主打 北海道浜中昆布湯底，湯頭清澈卻不單薄，越煮越能喝出海藻與柴魚的自然香氣。 用餐體驗整體氛圍偏家庭取向，桌距寬敞、座位舒適，帶小孩來也不覺擁擠。店員態度親切，補湯、收盤都很勤快，給人一種「被照顧著」的安心感。 綜合評分
地址：403臺中市西區公益路288號電話：0910855180 小結語加分100%浜中特選昆布鍋物是一間「不浮誇、但會讓人想再訪」的火鍋店。它不追求豪華擺盤，而是用最簡單的湯頭與新鮮食材，傳遞出家常卻不平凡的溫度。 印月餐廳｜中式料理的藝術演繹，宴客與家庭聚會首選
說到臺中公益路的中式料理代表，印月餐廳 絕對是榜上有名。這間開業多年的餐廳以「中菜西吃」的概念聞名，把傳統中式料理以現代手法重新詮釋。從建築外觀到餐具擺設，每個細節都散發著低調的典雅氣息。 餐點特色
印月最令人印象深刻的是他們將傳統中菜融入創意手法。 用餐體驗服務方面完全對得起餐廳的高級定位。從入座、點餐到上菜節奏，都拿捏得恰如其分。每道菜都會有服務人員細心介紹食材與吃法，讓人感受到「被款待」的尊榮感。 綜合評分
地址：408臺中市南屯區公益路二段818號電話：0422511155 小結語印月餐廳是一間「不只吃飯，更像品味生活」的地方。 KoDō 和牛燒肉｜極致職人精神，專為儀式感與頂級味覺而生
若要形容 KoDō 和牛燒肉 的用餐體驗，一句話足以總結——「像在欣賞一場關於肉的表演」。 餐點特色
這裡主打 日本A5和牛冷藏肉，以「精切厚燒」的方式呈現。 用餐體驗KoDō 的最大特色是「儀式感」。 綜合評分
地址：403臺中市西區公益路260號電話：0423220312 官網：https://www.facebook.com/kodo2018/ 小結語KoDō 和牛燒肉不是日常餐廳，而是一場體驗。 永心鳳茶｜在茶香裡用餐的優雅時光，臺味早午餐的新詮釋
走進 永心鳳茶公益店，彷彿進入一間有氣質的茶館。 餐點特色
永心鳳茶的餐點結合中式靈魂與西式擺盤，無論是「炸雞腿飯」還是「紅玉紅茶拿鐵」，都能讓人感受到熟悉卻不平凡的味道。 用餐體驗店內服務人員態度溫和，對茶品介紹詳盡。上餐節奏剛好，不急不徐。 綜合評分
地址：40360臺中市西區公益路68號三樓(勤美誠品)電話：0423221118 小結語永心鳳茶讓人重新定義「臺味」。 三希樓｜老饕級江浙功夫菜，穩重又帶人情味的中式饗宴
位於公益路上的 三希樓 是許多臺中老饕的口袋名單。 餐點特色
三希樓的菜色以 江浙與港式料理 為主，兼顧傳統與現代風味。 用餐體驗三希樓的服務給人一種老派但貼心的感覺。 綜合評分
地址：408臺中市南屯區公益路二段95號電話：0423202322 官網：https://www.sanxilou.com.tw/ 小結語三希樓是一間「吃得出功夫」的餐廳。 一笈壽司｜低調奢華的無菜單日料，職人手藝詮釋旬味極致
在熱鬧的公益路上，一笈壽司 低調得幾乎不顯眼。 餐點特色
一笈壽司採 Omakase（無菜單料理） 形式，每一餐都由主廚根據當日食材設計。 用餐體驗整場用餐約90分鐘，節奏緩慢但沉穩。 綜合評分
地址：408臺中市南屯區公益路二段25號電話：0423206368 官網：https://www.facebook.com/YIJI.sushi/ 小結語一笈壽司是一間真正讓人「放慢呼吸」的餐廳。 茶六燒肉堂｜人氣爆棚的和牛燒肉聖地，肉香與幸福感同時滿分
若要票選公益路上「最難訂位」的餐廳，茶六燒肉堂 絕對名列前茅。 餐點特色
茶六主打 和牛燒肉套餐，價格約落在 $700–$1000 間，份量與品質兼具。 用餐體驗茶六的服務效率相當高。店員親切、換網勤快、補水速度快，整場用餐流程流暢無壓力。 綜合評分
地址：403臺中市西區公益路268號電話：0423281167 官網：https://inline.app/booking/-L93VSXuz8o86ahWDRg0:inline-live-karuizawa/-LUYUEIOYwa7GCUpAFWA 小結語茶六燒肉堂用「穩定品質＋輕奢氛圍」抓住了臺中年輕族群的心。 吃完10家公益路餐廳後的心得與結語吃完這十家餐廳後，臺中公益路不只是一條美食街，而是一段生活風景線。 有的餐廳講究細膩與儀式感，像 一頭牛日式燒肉 與 一笈壽司，讓人感受到食材最純粹的美好 有的則以親切與溫度打動人心，像 加分昆布鍋物、永心鳳茶，讓人明白吃飯不只是為了飽足，而是一種被照顧的幸福。 而像茶六燒肉堂、TANG Zhan 湯棧 這類人氣名店，則用穩定的品質與熱絡的氛圍，成為許多臺中人心中「想吃肉就去那裡」的代名詞。 這十家店，構成了公益路最動人的縮影 有華麗的，也有溫柔的；有傳統的，也有創新的。 每一家都在自己的風格裡發光，讓人吃到的不只是料理，而是一種生活的溫度與節奏。 對我而言，這不僅是一場美食旅程，更是一趟關於「臺中味道」的回憶之旅。 FAQ：關於臺中公益路美食常見問題Q1：公益路哪一區的餐廳最集中？ Q2：需要提前訂位嗎？ 最後的話若要用一句話形容這趟美食之旅，我會說： 茶六燒肉堂長輩會喜歡嗎？ 如果你也和我一樣喜歡用味蕾探索一座城市，那就把這篇公益路美食攻略收藏起來吧。三希樓真的有那麼好吃嗎？ 無論是約會、慶生、家庭聚餐，或只是想犒賞一下辛苦的自己——這條路上永遠會有一間剛剛好的餐廳在等你。一笈壽司價格合理嗎？ 下一餐，不妨從這10家開始。加分100%浜中特選昆布鍋物長輩會喜歡嗎？ 打開手機、約上朋友，讓公益路成為你生活裡最容易抵達的小確幸。TANG Zhan 湯棧小孩適合去嗎？ 如果你有私心愛店，也歡迎留言分享，茶六燒肉堂份量足夠嗎？ 你的推薦，可能讓我下一趟美食旅程變得更精彩。KoDō 和牛燒肉適合跨年聚餐嗎？ One of the new OSD species – a hydrothermal vent limpet, Lepetodrilus marianae. Credit: Chong Chen, Hiromi Kayama Watanabe, and Miwako Tsuda Ocean biodiversity is under significant threat due to global changes, but new initiatives like the Ocean Species Discoveries, coordinated by the Senckenberg Ocean Species Alliance, aim to rapidly describe and publish findings on marine species. This innovative approach reduces the usual decades-long delay in species description, directly contributing to the conservation efforts needed to protect vulnerable marine habitats and their undiscovered inhabitants. Accelerating Biodiversity Research Accelerating global change continues to threaten Earth’s vast biodiversity, including in the oceans, which remain largely unexplored. To date, only a small fraction of an estimated two million total living marine species have been named and described. A major challenge is the time it takes to scientifically describe and publish a new species, which is a crucial step in studying and protecting these species. The current scientific and publishing landscape often results in decade-long delays (20-40 years) from the discovery of a new species to its official description. As an alternative to this, the Ocean Species Discoveries initiative was launched, offering a new platform for rapid but thorough taxonomic description of marine invertebrate species. One of the new OSD species – a deep-sea chiton, Placiphorella methanophila. Credit: Katarzyna Vončina Streamlining Species Discovery Ocean Species Discoveries is coordinated by the Senckenberg Ocean Species Alliance (SOSA), a project of the Senckenberg Research Institute and Natural History Museum Frankfurt. SOSA’s goal is to facilitate the discovery, protection, and awareness of marine invertebrate species before they become extinct. The project coordinated 25 different researchers and produced data on thirteen marine invertebrate taxa, including one new genus, eleven new species, and one redescription and reinstatement. The species, which originate from all over the globe and at depths from 5.2 to 7081 meters, are brought together in an open-access publication in the Biodiversity Data Journal. One of the new OSD species – a hole-making amphipod, Cunicolomaera grata. Credit: Anne Helene S. Tandberg and Anna M. Jażdżewska Rapid Response to Marine Threats This is the first of a series of publications related to SOSA’s initiative, in collaboration with Biodiversity Data Journal, presenting a revolutionary approach in new species descriptions, thanks to which the publication of new species takes years, sometimes even decades, less. The ARPHA publishing platform, which powers the Biodiversity Data Journal, further expedites species descriptions and their use in studies and conservation programs by employing a streamlined data publishing workflow. ARPHA automatically exports all species data, complete with images and descriptions, to GBIF—the Global Biodiversity Information Facility and the Biodiversity Literature Repository at Zenodo, from where other researchers can easily find and use them. The reinstated OSD species – a purple long-tailed sea cucumber, Psychropotes buglossa. Credit: Amanda Serpell-Stevens, Tammy Horton, and Julia Sigwart Discovering Deep-Sea Dwellers One of the new species described in the Ocean Species Discoveries is Cunicolomaera grata, a curious amphipod whose burrows along the seafloor perplexed scientists. Another is a wrinkly-shelled limpet called Lepetodrilus marianae that lives on hydrothermal vents, underwater volcanoes in the deep-sea where temperatures can reach 400 degrees C. Normally, the descriptions for these two very different species wouldn’t be in the same publication, but this new publication format allows for species descriptions from different marine invertebrate taxa to be published together in one ‘mega-publication,’ offering a huge incentive for researchers to make their discoveries public. Highlighting Taxonomy’s Role in Conservation “Currently, there’s a notable delay in naming and describing new animals, often because journals expect additional ecological or phylogenetic insights. This means many marine species go undescribed due to lack of data. OSD addresses this by offering concise, complete taxonomic descriptions without requiring a specific theme, refocusing attention on taxonomy’s importance,” says Dr. Torben Riehl, who is one of the researchers featured in Ocean Species Discoveries. Leveraging Global Expertise for Ocean Health Reducing the time it takes to get from discovering a new animal to a public species description is crucial in our era of increasing biodiversity loss. The wrinkly-shelled limpet and two other species described in the Ocean Species Discoveries live in hydrothermal vent zones – an environment threatened by deep-sea mining. Another OSD species, Psychropotes buglossa, a purple sea cucumber (sometimes also called a gummy squirrel), lives in the North Atlantic, but similar species live in areas of high economic interest, where polymetallic-nodule extraction could soon endanger sea life. Threats like these risk driving species to extinction before we even get the chance to know and study them. Through efforts like SOSA’s Ocean Species Discoveries, we can get closer to understanding the biodiversity of our oceans and protecting it before it’s too late. A Call to Marine Taxonomists “Only by leveraging the collective strengths of global progress, expertise, and technological advancements, will we be able to describe the estimated 1.8 million unknown species living in our oceans. Every taxonomist specialized on some group of marine invertebrates is invited to contribute to the Ocean Species Discoveries,” says Prof. Dr. Julia Sigwart in conclusion. Reference: “Ocean Species Discoveries 1-12 — A primer for accelerating marine invertebrate taxonomy” by Senckenberg Ocean Species Alliance (SOSA), Angelika Brandt, Chong Chen, Laura Engel, Patricia Esquete, Tammy Horton, Anna M. Jażdżewska, Nele Johannsen, Stefanie Kaiser, Terue C. Kihara, Henry Knauber, Katharina Kniesz, Jannes Landschoff, Anne-Nina Lörz, Fabrizio M. Machado, Carlos A. Martínez-Muñoz, Torben Riehl, Amanda Serpell-Stevens, Julia D. Sigwart, Anne Helene S. Tandberg, Ramiro Tato, Miwako Tsuda, Katarzyna Vončina, Hiromi K. Watanabe, Christian Wenz and Jason D. Williams, 6 August 2024, Biodiversity Data Journal. DOI: 10.3897/BDJ.12.e128431 The neuroactivity of one million neurons in the mouse brain, at unprecedented resolution. Credit: Alipasha Vaziri New microscopy technique reveals activity of one million neurons across the mouse brain. Capturing the intricacies of the brain’s activity demands resolution, scale, and speed—the ability to visualize millions of neurons with crystal clear resolution as they actively call out from distant corners of the cortex, within a fraction of a second of one another. Now, researchers have developed a microscopy technique that will allow scientists to accomplish this feat, capturing detailed images of activity of a vast number of cells across different depths in the brain at high speed and with unprecedented clarity. Published in Nature Methods, the research demonstrates the power of this innovation, dubbed light beads microscopy, by presenting the first vivid functional movies of the near-simultaneous activity of one million neurons across the mouse brain. “Understanding the nature of the brain’s densely interconnected network requires developing novel imaging techniques that can capture the activity of neurons across vastly separated brain regions at high speed and single-cell resolution,” says Rockefeller’s Alipasha Vaziri. “Light beads microscopy will allow us to investigate biological questions in a way that had not been possible before.” A focus on microscopy Whether it’s whiskers that seek hazards by flicking to and fro, or hand-eye-coordination that helps a human hit a baseball, animals rely upon the call and response of the sensory, motor, and visual regions of the brain. Cells from far reaches of the cortex coordinate this feat through a web of neuroactivity that weaves distant regions of the brain into interconnected symphonies. Scientists are only now beginning to untangle this web, with the help of cutting-edge microscope technology. The combination of two-photon scanning microscopy and fluorescent tags is the gold standard when it comes to imaging the activity of neurons within less transparent brain tissues, which are prone to scattering light. It involves firing a focused laser pulse at a tagged target. A few nanoseconds after the pulse hits its mark, the tag emits fluorescent light that can be interpreted to give scientists an idea of the level of neuroactivity detected. But two-photon microscopy suffers from a fundamental limitation. Neurobiologists need to record simultaneous interactions between the sensory, motor, and visual regions of the brain, but it is difficult to capture the activity in such a broad swath of the brain without sacrificing resolution or speed. Designing an ideal microscope for visualizing interactions between far apart brain regions can feel like plugging holes in a sinking ship. In the interests of high resolution, scientists often must sacrifice scale—or zoom out to take in the larger structure, at the cost of resolution. This can be overcome by snapping a series of high-resolution images from distant corners of the brain separately, later stitching them together. But then speed becomes an issue. “We need to capture many neurons at distant parts of the brain at the same time at high resolution,” Vaziri says. “These parameters are almost mutually exclusive.” An innovative resolution Light beads microscopy offers a creative solution and pushes the limits of imaging speed to what’s maximally obtainable – only limited by physical nature of fluorescence itself. This is done by eliminating the “deadtime” between sequential laser pulses when no neuroactivity is recorded and at the same time the need for scanning. The technique involves breaking one strong pulse into 30 smaller sub pulses – each at a different strength – that dive into 30 different depths of scattering mouse brain but induce the same amount of fluorescence at each depth. This is accomplished with a cavity of mirrors that staggers the firing of each pulse in time and ensures that they can all reach their target depths via a single microscope focusing lens. With this approach, the only limit to the rate at which samples can be recorded is the time that it takes the fluorescent tags to flare. That means broad swaths of the brain can be recorded within the same time it would take a conventional two-photon microscope to capture a mere smattering of brain cells. Vaziri and colleagues then put light beads microscopy to the test by integrating it into a microscopy platform that allows for optical access to a large brain volume enabling the recording of the activity of more than one million neurons across the entire cortex of the mouse brain for the first time. Because Vaziri’s method is an innovation that builds on two photon microscopy, many labs already have or can commercially obtain the technologies necessary to perform light beads microscopy, as described in the paper. Labs that are less familiar with these techniques could benefit from a simplified, self-contained module that Vaziri is currently developing for more widespread use. “There’s no good reason why we didn’t do this five years ago,” he says. “It would have been possible—the microscope and laser technology existed. No one thought of it.” Ultimately, the goal is to complement rather than replace current techniques. “There are neurobiological questions for which the standard two-photon microscope is sufficient,” Vaziri says. ” But light beads microscopy allows us to address questions that existing methods cannot.” Reference: “High-speed, cortex-wide volumetric recording of neuroactivity at cellular resolution using light beads microscopy” by Jeffrey Demas, Jason Manley, Frank Tejera, Kevin Barber, Hyewon Kim, Francisca Martínez Traub, Brandon Chen and Alipasha Vaziri, 30 August 2021, Nature Methods. DOI: 10.1038/s41592-021-01239-8 Researchers have developed a biomaterial vaccine formulation that significantly enhances and extends lymph node expansion, leading to improved immune responses and vaccine efficacy against tumors. By jump-starting LN expansion before administering a traditional vaccine, they achieved more effective and sustained anti-tumor responses. A new study reveals that enhanced lymph node expansion from biomaterial vaccines could boost tumor vaccine efficacy, potentially revolutionizing future vaccine developments. The human body has approximately 600 lymph nodes (LNs). These small, bean-shaped organs house various types of blood cells and filter lymph fluid. Vaccines can cause the LNs near an injection site to temporarily expand, a phenomenon that is thought to reflect an ongoing vaccine immune response. Although researchers have studied the early expansion of LNs following vaccination, they have not investigated whether prolonged LN expansion could affect vaccine outcomes. New Research Findings Now scientists have found a way to enhance and extend LN expansion and study how this phenomenon affects both the immune system and efficacy of vaccinations against tumors. In a revolutionary approach, researchers used a biomaterial vaccine formulation that enabled greater and more persistent LN expansion than standard control vaccines. While the oversized LNs maintained a normal tissue organization, they displayed altered mechanical features and hosted higher numbers of various immune cell types that commonly are involved in immune responses against pathogens and cancers. Notably, “jump-starting” lymph node expansion prior to administering a traditional vaccine against a melanoma-specific model antigen led to more effective and sustained anti-tumor responses in mice. This immunofluorescent staining shows a lymph node that has been significantly expanded in mice with the help of the biomaterial MPS-vaccine (on the right), next to a lymph node taken from non-treated control mice (on the left) at the same time post-vaccination. Credit: Wyss Institute at Harvard University This groundbreaking research was conducted by scientists from the Wyss Institute for Biologically Inspired Engineering at Harvard University, Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS), and Genentech, a member of the Roche Group. The findings are published in Nature Biomedical Engineering. Study Details and Implications “By enhancing the initial and sustained expansion of LNs with biomaterial scaffolds, non-invasively monitoring them individually over long time periods, and probing deeply into their tissue architecture and immune cell populations, we tightly correlate a persistent LN expansion with more robust immune and vaccination responses,” said Wyss Institute Founding Core Faculty member David Mooney, Ph.D., who led the study. “This opens a new front of investigation for immunologists, and could have far-reaching implications for future vaccine developments.” The authors used a method know as high-frequency ultrasound to monitor individual lymph nodes in MPS- and control-vaccinated mice. The top row shows a series of lymph nodes on day 7 following MPS vaccination. All of them were significantly expanded, compared to lymph nodes following control vaccination imaged at the same time and shown in the bottom row. Credit: Wyss Institute at Harvard University Previous Work and New Discoveries Mooney’s team at the Wyss Institute and SEAS had previously developed different biomaterial scaffolds as a matrix for cancer and infection vaccines. The researchers have demonstrated the potential of biomaterial vaccine formulations to successfully fight the growth of tumors in an extensive body of work performed in preclinical animal models and a first clinical trial with cancer patients. But they hadn’t yet investigated how their vaccines and those developed by others could influence the response of LNs draining leaked tissue fluid at vaccine injection sites, and have an impact on the LNs tissue organization, different cell types, and their gene expression, which could in turn affect vaccine efficacy. In their new study, they tested a previously developed vaccine formulation that is based on microscale mesoporous silica (MPS) rods that can be injected close to tumors and form a cell-permeable 3D scaffold structure under the skin. Engineered to release an immune cell-attracting cytokine (GM-CSF), and immune cell-activating adjuvant (CpG), and tumor-antigen molecules, MPS-vaccines are able to reprogram recruited so-called antigen-presenting cells that, upon migrating into nearby LNs, orchestrate complex tumor cell-killing immune responses. Their new study showed that there are more facets to that concept. “As it turns out, the immune-boosting functions of basic MPS-vaccines actively change the state of LNs by persistently enlarging their whole organ structure, as well as changing their tissue mechanics and immune cell populations and functions,” said first-author Alexander Najibi, Ph.D., who performed his Ph.D. thesis with Mooney. Probing LNs With Ultra-Sound and Nano-Devices To understand the response of LNs to MPS-vaccines over time, the team applied an ultra-sound imaging technique known as high-frequency ultrasound (HFUS). Similar to monitoring a tiny fetus developing in a mother’s womb by clinical ultra-sound, HFUS, on a much smaller scale, enables non-invasively and non-destructively monitoring of anatomical details of tissues and organs in small animals such as mice. Using HFUS, the team traced individual LNs in MPS-vaccinated mice over 100 days. They identified an initial peak expansion period that lasted until day 20, in which LN volumes increased about 7-fold, significantly greater than in animals that received traditional vaccine formulations. Importantly, the LNs of MPS-vaccinated mice, while decreasing in volumes after this peak expansion, remained significantly more expanded than LNs from traditionally vaccinated mice throughout the 100-day time course. When Najibi and the team investigated the mechanical responses of the LNs using a nanoindentation device, they found that LNs in MPS-vaccinated animals, although maintaining an overall normal structure, were less stiff and more viscous in certain locations. This was accompanied by a re-organization of a protein that assembles and controls cells’ mechanically active cytoskeleton. Interestingly, Mooney’s group had shown in an earlier biomaterial study that changing mechanical features of immune cells’ environments, especially their viscoelasticity, affects immune cell development and functions. “It is very well-possible that in order to accommodate the significant growth induced by MPS-vaccines, LNs need to become softer and more viscous, and that this then further impacts immune cell recruitment, proliferation, and differentiation in a feed-forward process,” said Najibi. From Immune Cell Engagement to Vaccine Responses Interestingly, upon MPS-vaccination, the numbers of “innate immune cells,” including monocytes, neutrophils, macrophages, and other cell types that build up the first wave of immune defenses against pathogens and unwanted cells, peaked first in expanding LNs. Peaking with a delay were dendritic cells (DCs), which normally transfer information in the form of antigens from invading pathogens and cancer cells to “adaptive immune cells” that then launch subsequent waves of highly specific immune responses against the antigen-producing invaders. In fact, along with DCs, also T and B cell types of the adaptive immune system started to reach their highest numbers. “It was fascinating to see how the distinct changes in immune cell populations that we detected in expanding LNs in response to the MPS-vaccine over time re-enacted a typical immune response to infectious pathogens,” commented Najibi. Innate immune cells and DCs are also known as “myeloid cells,” which are known to interact with LN tissue during early expansion. To further define the impact of myeloid cells on LN expansion, Mooney’s team collaborated with the group of Shannon Turley, Ph.D., the VP of Immunology and Regenerative Medicine at Genentech, and an expert in lymph node biology and tumor immunology. “The MPS-vaccine led to extraordinary structural and cellular changes within the lymph node that supported potent antigen-specific immunity,” said Turley. By isolating myeloid cells from LNs and analyzing the gene expression profiles of individual cells (single-cell RNA-seq), the groups were able to reconstruct distinct changes in myeloid cell populations during LN expansion and identified distinct DC populations in durably expanded LNs whose changed gene expression was associated with LN expansion. In addition, the collaborators found that the number of monocytes increased 80-fold upon MPS-vaccination – the highest increase among all myeloid cell types – and pinpointed subpopulations of “inflammatory and antigen-presenting monocytes” as promising candidates for facilitating LN expansion. In fact, when they depleted specific subpopulations of these types of monocytes from circulating blood of mice after vaccination, the maintenance of LN expansion, and timing of the T cell response to vaccination, were altered. Enhancing Vaccine Effectiveness The team explored whether LN expansion could enhance the effectiveness of vaccination. “Jump-starting” the immune system in LNs with an antigen-free MPS-vaccine and subsequently administering the antigen in a traditional vaccine format significantly improved anti-tumor immunity and prolonged the survival of melanoma-bearing mice, compared to the traditional vaccine alone. “The priming of lymph nodes for subsequent vaccinations using various formulations could be a low-hanging fruit for future vaccine developments,” said Mooney. “This newfound ability to physically expand lymph nodes and enhance their various immune activities over longer treatment courses, using cleverly designed and easy-to-administer biomaterials, could provide a tremendous push to immunotherapies in patients. It is also yet another great example of how mechanics plays a key role in regulation of living systems, even immune responses where few would consider physical cues to be important,” said Wyss Founding Director Donald Ingber, M.D., Ph.D., who is also the Judah Folkman Professor of Vascular Biology at Harvard Medical School and Boston Children’s Hospital, and the Hansjörg Wyss Professor of Bioinspired Engineering at SEAS. Reference: “Durable lymph-node expansion is associated with the efficacy of therapeutic vaccination” by Alexander J. Najibi, Ryan S. Lane, Miguel C. Sobral, Giovanni Bovone, Shawn Kang, Benjamin R. Freedman, Joel Gutierrez Estupinan, Alberto Elosegui-Artola, Christina M. Tringides, Maxence O. Dellacherie, Katherine Williams, Hamza Ijaz, Sören Müller, Shannon J. Turley and David J. Mooney, 6 May 2024, Nature Biomedical Engineering. DOI: 10.1038/s41551-024-01209-3 Other authors of the study are Ryan Lane, Miguel Sobral, Giovanni Bovone, Shawn Kang, Benjamin Freedman, Joel Gutierrez Estupinan, Alberto Elosegui-Artola, Christina Tringides, Maxence Dellacherie, Katherine Williams, Hamza Ijaz, and Sören Müller. The study was funded by the National Institutes of Health/National Cancer Institute (award# U54 CA244726 and R01 CA223255). RRG455KLJIEVEWWF 永心鳳茶值得推薦嗎？ 》台中公益路高分美食推薦｜10間絕對不踩雷一笈壽司肉質如何？ 》台中公益路食記攻略｜10家餐廳評分&推薦茶六燒肉堂好吃嗎？ 》台中公益路吃爆指南｜10家餐廳逐間介紹 |
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